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Standard

Sodium/potassium-transporting ATPase subunit beta-1 levels

GPLD1 · rs60816578

Strength of the evidence

3 / 4

Its strongest genetic-study result is p = 10−52, 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 10,708 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.268 higher (95% confidence interval 0.23-0.3); p = 6 × 10−53.

How common The A allele had a frequency of about 85% in the people studied.

Where it sits Chromosome 6, band 6p22.3 — in an intron of GPLD1.

How common each version is

AG
Korean KRGDB
A 91.4% · G 8.6%
Korean Korea4K
A 91.3% · G 8.6%
Korean Korea1K
A 91.6% · G 8.3%
Japanese ToMMo
A 93.5% · G 6.5%
Vietnamese
A 91.1% · G 8.9%
World gnomAD
A 80.8% · G 19.2%
World 1000 Genomes
A 79.7% · G 20.3%
World TOPMed
A 80.7% · G 19.3%

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.

What each result means

A/A Two copies of the version the research linked to Sodium/potassium-transporting ATPase subunit beta-1 levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/G One copy of the version the research linked to Sodium/potassium-transporting ATPase subunit beta-1 levels. That is a smaller link than two copies.
G/G No copy of the version the research linked to Sodium/potassium-transporting ATPase subunit beta-1 levels. This is the starting point the study compared everyone against.
Source

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Sodium/potassium-transporting ATPase subunit beta-1 levels (rs60816578). MyGeneLog™. https://www.mygenelog.com/variants/rs60816578

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