rs374163823
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs374163823(A;A) |
Make rs374163823(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 16 |
Position | 56879593 |
Gene | SLC12A3 |
is a | snp |
is | mentioned by |
dbSNP | rs374163823 |
dbSNP (classic) | rs374163823 |
ClinGen | rs374163823 |
ebi | rs374163823 |
HLI | rs374163823 |
Exac | rs374163823 |
Gnomad | rs374163823 |
Varsome | rs374163823 |
LitVar | rs374163823 |
Map | rs374163823 |
PheGenI | rs374163823 |
Biobank | rs374163823 |
1000 genomes | rs374163823 |
hgdp | rs374163823 |
ensembl | rs374163823 |
geneview | rs374163823 |
scholar | rs374163823 |
rs374163823 | |
pharmgkb | rs374163823 |
gwascentral | rs374163823 |
openSNP | rs374163823 |
23andMe | rs374163823 |
SNPshot | rs374163823 |
SNPdbe | rs374163823 |
MSV3d | rs374163823 |
GWAS Ctlg | rs374163823 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs374163823(A;A) |
Alt | rs374163823(A;A) |
Reference | Rs374163823(G;G) |
Significance | Pathogenic |
Disease | Familial hypokalemia-hypomagnesemia not provided |
Variation | info |
Gene | SLC12A3 |
CLNDBN | Familial hypokalemia-hypomagnesemia not provided |
Reversed | 0 |
HGVS | NC_000016.9:g.56913505G>A |
CLNSRC | |
CLNACC | RCV000286818.1, RCV000414425.1, |