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Gene

PTCH1

PTCH1 is a gene. This site has 87 published variants inside it and 24 near it, each from a published genetic study, joining it to 16 condition pages.

Conditions it is linked to

• Adventurousness
• Basal Cell Carcinoma
• Birth Weight
• Blood Cell Counts
• Blood Pressure
• Breast Cancer
• Height
• Hip Circumference
• IgG4-Related Disease
• Ischaemic Stroke
• Knee Osteoarthritis
• Migraine
• Neuroticism
• Obesity and Body Weight
• Osteoarthritis
• Pulmonary Function (Lung Capacity)

Variants inside PTCH1 (87)

• rs73529860 · Adventurousness
• rs28629854 · Anterior amygdaloid area volume
• rs145922731 · Appendicular lean mass
• rs191458964 · Appendicular lean mass
• rs1840094606 · Basal cell carcinoma, susceptibility to, 1
• rs28510415 · Birth weight
• rs28701981 · Body shape phenotype PC2
• rs28496034 · Cortical surface area
• rs3758301 · Diastolic blood pressure
• rs113154802 · Forced vital capacity (FVC)
• rs1060502277 · Gorlin syndrome
• rs1060502282 · Gorlin syndrome
• rs1064793921 · Gorlin syndrome
• rs1064793922 · Gorlin syndrome
• rs1064793978 · Gorlin syndrome
• rs1085307511 · Gorlin syndrome
• rs1085307752 · Gorlin syndrome
• rs1268572514 · Gorlin syndrome
• rs1333346461 · Gorlin syndrome
• rs1344258746 · Gorlin syndrome
• rs1554692291 · Gorlin syndrome
• rs1554702186 · Gorlin syndrome
• rs1564055259 · Gorlin syndrome
• rs1587692888 · Gorlin syndrome
• rs1588528503 · Gorlin syndrome
• rs1588574709 · Gorlin syndrome
• rs1588605348 · Gorlin syndrome
• rs1588614178 · Gorlin syndrome
• rs1838315058 · Gorlin syndrome
• rs1838655420 · Gorlin syndrome
• rs1841170844 · Gorlin syndrome
• rs1843665508 · Gorlin syndrome
• rs2118020615 · Gorlin syndrome
• rs2118391725 · Gorlin syndrome
• rs2118420718 · Gorlin syndrome
• rs2118429101 · Gorlin syndrome
• rs2118471978 · Gorlin syndrome
• rs2118873472 · Gorlin syndrome
• rs2538216536 · Gorlin syndrome
• rs2538216680 · Gorlin syndrome
• rs2538217131 · Gorlin syndrome
• rs376353501 · Gorlin syndrome
• rs774822170 · Gorlin syndrome
• rs863224347 · Gorlin syndrome
• rs863224444 · Gorlin syndrome
• rs863225054 · Gorlin syndrome
• rs864622088 · Gorlin syndrome
• rs864622120 · Gorlin syndrome
• rs864622293 · Gorlin syndrome
• rs878853849 · Gorlin syndrome
• rs878853856 · Gorlin syndrome
• rs28442014 · Height
• rs473902 · Height
• rs148786069 · Height (baseline)
• rs28446321 · Hemoglobin levels
• rs1060502268 · Hereditary cancer-predisposing syndrome
• rs1060502301 · Hereditary cancer-predisposing syndrome
• rs1064794260 · Hereditary cancer-predisposing syndrome
• rs1131690968 · Hereditary cancer-predisposing syndrome
• rs1131690985 · Hereditary cancer-predisposing syndrome
• rs1131690986 · Hereditary cancer-predisposing syndrome
• rs1131690992 · Hereditary cancer-predisposing syndrome
• rs1131690995 · Hereditary cancer-predisposing syndrome
• rs142340833 · Hereditary cancer-predisposing syndrome
• rs1588602262 · Hereditary cancer-predisposing syndrome
• rs766313615 · Hereditary cancer-predisposing syndrome
• rs781768965 · Hereditary cancer-predisposing syndrome
• rs145965565 · Hip circumference adjusted for BMI
• rs16909865 · Hip circumference adjusted for BMI
• rs28704635 · Hip circumference adjusted for BMI
• rs481237 · Hip circumference adjusted for BMI
• rs568513587 · Hip circumference adjusted for BMI
• rs663344 · Hip circumference adjusted for BMI
• rs76239439 · Hip circumference adjusted for BMI
• rs2274692 · Hippocampal subfield left CA1 volume (body)
• rs1554691359 · Inborn genetic diseases
• rs1554698260 · Inborn genetic diseases
• rs79057214 · Knee osteoarthritis
• rs28713678 · Liver enzyme levels (alkaline phosphatase)
• rs10512249 · Neuroticism
• rs75614054 · Neuroticism
• rs2066831 · PTCH1-related disorder
• rs28583690 · Red blood cell count
• rs2282040 · Sensitivity to environmental stress and adversity
• rs2405134 · Serum alkaline phosphatase levels
• rs28457763 · Vertex-wise sulcal depth
• rs28427480 · Well-being spectrum (multivariate analysis)

Variants near PTCH1 (24)

Positions outside the gene, filed under it because it is the closest. A variant near a gene does not always act through it.

• rs182923402 · Anterior amygdaloid area volume
• rs73654566 · DXA-Bone mineral density (lumbar spine)
• rs10120432 · Estrogen-receptor positive breast cancer
• rs10512247 · Height
• rs16909859 · Height
• rs17370391 · Height
• rs28393820 · Height
• rs28536742 · Height
• rs28778940 · Height
• rs56119276 · Height
• rs117023826 · Height (baseline)
• rs118043221 · Height (baseline)
• rs34887715 · Height (baseline)
• rs28453815 · Hemoglobin concentration
• rs66917126 · IgG4-related Mikuliczs disease
• rs76597087 · Migraine
• rs112191650 · Neuroticism
• rs78893982 · Neuroticism
• rs76340814 · Osteoarthritis of the hip or knee (with total joint replacement)
• rs34592343 · Physical function (baseline)
• rs2405068 · Small vessel stroke
• rs28697937 · Standing height (UKB data field 50)
• rs16909923 · Weight
• rs113502615 · Whole body fat free mass (UKB data field 23101)

See PTCH1 with everything it connects to on the Gene Knowledge Graph, or as data at /api/v1/genes/PTCH1.

A gene page gathers published research; it is not a test result and not medical advice. If a gene matters to your health, talk to a doctor or a genetic counsellor.