Standard

Waist-hip ratio

HMBS · rs1006195

Where this position leads

Condition: Waist-to-Hip Ratio (Body Fat Distribution)

rs1006195 Condition: Waist-to-Hip Ratio (Body Fat Distribution) Waist-to-Hip Ratio (Body Fat Distri… Condition rs1006195 rs1006195 HMBS

What the study found

Who was studied 381,152 European female individuals.

The effect Each copy of the T allele shifted the measure 0.0139 higher (95% confidence interval 0.01-0.017); p = 3 × 10−14.

How common The T allele had a frequency of about 39% in the people studied.

Where it sits Chromosome 11, band 11q23.3 — in an intron of HMBS.

What ClinVar records

Classification Benign; criteria provided, multiple submitters, no conflicts (2 of 4 stars, 2 submitters), last evaluated 2021-06-19. ClinVar record 1246575 NM_000190.4(HMBS):c.34-96G>T

What this is ClinVar's aggregate record for this position (as of its 2026-10-12 release), not a result about you. A classification describes the variant against the condition named, as laboratories submitted it. Whether a person carries this variant, and what that would mean for them, is a question for a clinical test and a genetic counsellor.

What each result means

G/G No copy of the version the research linked to Waist-hip ratio. This is the starting point the study compared everyone against.
G/T One copy of the version the research linked to Waist-hip ratio. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Waist-hip ratio. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs1006195

What is rs1006195?

rs1006195 is a single position in the genome, in or near the HMBS gene. Published research associates it with waist-hip ratio. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs1006195 linked to?

On MyGeneLog this position is linked to Waist-to-Hip Ratio (Body Fat Distribution). The research behind each link, and its sources, are set out on that condition page.

Does having rs1006195 mean I will get this?

No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.

Where does the information about rs1006195 come from?

GWAS Catalog, Human molecular genetics 2019, PMID:30239722. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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Waist-hip ratio (rs1006195). MyGeneLog™. https://www.mygenelog.com/variants/rs1006195

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