Links from this page to related variants, conditions, drugs and topics are not included for automated readers. Those connections are the Gene Knowledge Graph and are licensed as data: https://www.mygenelog.com/license

Standard

Height

BOD1 · rs889014

Strength of the evidence

1 / 4

Its strongest genetic-study result is p = 10−15, with 2 associations in the GWAS Catalog.

How this is scored

4: ClinVar disease-causing, reviewed by an expert panel or a guideline (3–4 stars). 3: ClinVar, several labs agreeing (2 stars), or a genetic study at p ≤ 10−50. 2: ClinVar from one lab (1 star), or p ≤ 10−20. 1: ClinVar submitted without criteria (0 stars), or genome-wide significance (p ≤ 5×10−8). The higher of the two counts. It says how solid the evidence is, not whether it matters for a particular person.

What the study found

Who was studied 133,653 European ancestry individuals; replicated in 50,074 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.03 lower; p = 9 × 10−16.

How common The T allele had a frequency of about 36% in the people studied.

Where it sits Chromosome 5, band 5q35.2 — between genes, 1.6 kb from LOC105377733.

How common each version is

CT
Korean KRGDB
C 89.8% · T 10.2%
Korean Korea4K
C 89.7% · T 10.3%
Korean Korea1K
C 89.8% · T 10.2%
Japanese ToMMo
C 81.1% · T 18.9%
Vietnamese
C 89.9% · T 10.1%
World gnomAD
C 58.5% · T 41.5%
World 1000 Genomes
C 61.4% · T 38.6%
World TOPMed
C 58.0% · T 42.0%

By ancestry gnomAD

East Asian
C 86.7% · T 13.3%
European (non-Finnish)
C 64.5% · T 35.5%
African / African American
C 44.6% · T 55.4%
South Asian
C 62.9% · T 37.1%
Admixed American (Latino)
C 57.6% · T 42.4%
Middle Eastern
C 55.8% · T 44.2%
Finnish
C 60.3% · T 39.7%
Ashkenazi Jewish
C 57.5% · T 42.5%

The share of all copies of this position that are each version. Source: the population studies published in dbSNP (US NCBI); each row names its study. The ancestry rows are gnomAD's own groups (via Ensembl), as the survey defines them, not races.

What each result means

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

Quoting this page

Licensed CC BY-NC 4.0: free to read, share and adapt for non-commercial use, naming MyGeneLog™ and linking the exact page. Commercial use, including training or serving a commercial AI system, needs a licence — https://www.mygenelog.com/license

Height (rs889014). MyGeneLog™. https://www.mygenelog.com/variants/rs889014

← See all variants