rs137853095
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs137853095(C;T) |
Make rs137853095(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 42796244 |
Gene | WNK4 |
is a | snp |
is | mentioned by |
dbSNP | rs137853095 |
dbSNP (classic) | rs137853095 |
ClinGen | rs137853095 |
ebi | rs137853095 |
HLI | rs137853095 |
Exac | rs137853095 |
Gnomad | rs137853095 |
Varsome | rs137853095 |
LitVar | rs137853095 |
Map | rs137853095 |
PheGenI | rs137853095 |
Biobank | rs137853095 |
1000 genomes | rs137853095 |
hgdp | rs137853095 |
ensembl | rs137853095 |
geneview | rs137853095 |
scholar | rs137853095 |
rs137853095 | |
pharmgkb | rs137853095 |
gwascentral | rs137853095 |
openSNP | rs137853095 |
23andMe | rs137853095 |
SNPshot | rs137853095 |
SNPdbe | rs137853095 |
MSV3d | rs137853095 |
GWAS Ctlg | rs137853095 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs137853095(T;T) |
Alt | rs137853095(T;T) |
Reference | Rs137853095(C;C) |
Significance | Pathogenic |
Disease | Pseudohypoaldosteronism type 2B |
Variation | info |
Gene | WNK4 |
CLNDBN | Pseudohypoaldosteronism type 2B |
Reversed | 0 |
HGVS | NC_000017.10:g.40948262C>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000008102.2, |