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Standard

Serum alkaline phosphatase levels

GPLD1 · rs78420872

Strength of the evidence

3 / 4

Its strongest genetic-study result is p = 10−96, with 1 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 118,886 East Asian ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.166 lower (95% confidence interval 0.15-0.18); p = 4 × 10−97.

How common The A allele had a frequency of about 6% in the people studied.

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

How common each version is

AC
Korean KRGDB
A 8.1% · C 91.9%
Korean Korea4K
A 7.7% · C 92.3%
Korean Korea1K
A 7.7% · C 92.3%
Japanese ToMMo
A 6.5% · C 93.5%
Vietnamese
A 10.8% · C 89.2%
World gnomAD
A 9.3% · C 90.7%
World 1000 Genomes
A 9.7% · C 90.3%
World TOPMed
A 8.2% · C 91.8%

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

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Serum alkaline phosphatase levels (rs78420872). MyGeneLog™. https://www.mygenelog.com/variants/rs78420872

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