rs121912625
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs121912625(C;T) |
Make rs121912625(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 74840146 |
Gene | TRPM6 |
is a | snp |
is | mentioned by |
dbSNP | rs121912625 |
dbSNP (classic) | rs121912625 |
ClinGen | rs121912625 |
ebi | rs121912625 |
HLI | rs121912625 |
Exac | rs121912625 |
Gnomad | rs121912625 |
Varsome | rs121912625 |
LitVar | rs121912625 |
Map | rs121912625 |
PheGenI | rs121912625 |
Biobank | rs121912625 |
1000 genomes | rs121912625 |
hgdp | rs121912625 |
ensembl | rs121912625 |
geneview | rs121912625 |
scholar | rs121912625 |
rs121912625 | |
pharmgkb | rs121912625 |
gwascentral | rs121912625 |
openSNP | rs121912625 |
23andMe | rs121912625 |
SNPshot | rs121912625 |
SNPdbe | rs121912625 |
MSV3d | rs121912625 |
GWAS Ctlg | rs121912625 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121912625(T;T) |
Alt | rs121912625(T;T) |
Reference | Rs121912625(C;C) |
Significance | Pathogenic |
Disease | Hypomagnesemia 1 |
Variation | info |
Gene | TRPM6 |
CLNDBN | Hypomagnesemia 1, intestinal |
Reversed | 1 |
HGVS | NC_000009.11:g.77455062G>A |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000003768.4, |