rs3750425
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs3750425(C;T) |
Make rs3750425(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 74762494 |
Gene | TRPM6 |
is a | snp |
is | mentioned by |
dbSNP | rs3750425 |
dbSNP (classic) | rs3750425 |
ClinGen | rs3750425 |
ebi | rs3750425 |
HLI | rs3750425 |
Exac | rs3750425 |
Gnomad | rs3750425 |
Varsome | rs3750425 |
LitVar | rs3750425 |
Map | rs3750425 |
PheGenI | rs3750425 |
Biobank | rs3750425 |
1000 genomes | rs3750425 |
hgdp | rs3750425 |
ensembl | rs3750425 |
geneview | rs3750425 |
scholar | rs3750425 |
rs3750425 | |
pharmgkb | rs3750425 |
gwascentral | rs3750425 |
openSNP | rs3750425 |
23andMe | rs3750425 |
SNPshot | rs3750425 |
SNPdbe | rs3750425 |
MSV3d | rs3750425 |
GWAS Ctlg | rs3750425 |
GMAF | 0.1387 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 19149903] 4.9x risk of type-2 diabetes among women carriers of both the rare alleles at rs3750425 and rs2274924 when their magnesium intake was lower than 250 mg per day.
ClinVar | |
---|---|
Risk | rs3750425(A;A) rs3750425(T;T) |
Alt | rs3750425(A;A) rs3750425(T;T) |
Reference | Rs3750425(C;C) |
Significance | Non-pathogenic |
Disease | Hypomagnesemia 1 |
Variation | info |
Gene | TRPM6 |
CLNDBN | Hypomagnesemia 1, intestinal |
Reversed | 0 |
HGVS | NC_000009.11:g.77377410C>T |
CLNSRC | |
CLNACC | RCV000313266.1, |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 9
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d