rs137853342
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs137853342(A;A) |
Make rs137853342(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 23215237 |
Gene | SCNN1G |
is a | snp |
is | mentioned by |
dbSNP | rs137853342 |
dbSNP (classic) | rs137853342 |
ClinGen | rs137853342 |
ebi | rs137853342 |
HLI | rs137853342 |
Exac | rs137853342 |
Gnomad | rs137853342 |
Varsome | rs137853342 |
LitVar | rs137853342 |
Map | rs137853342 |
PheGenI | rs137853342 |
Biobank | rs137853342 |
1000 genomes | rs137853342 |
hgdp | rs137853342 |
ensembl | rs137853342 |
geneview | rs137853342 |
scholar | rs137853342 |
rs137853342 | |
pharmgkb | rs137853342 |
gwascentral | rs137853342 |
openSNP | rs137853342 |
23andMe | rs137853342 |
SNPshot | rs137853342 |
SNPdbe | rs137853342 |
MSV3d | rs137853342 |
GWAS Ctlg | rs137853342 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs137853342(A;A) |
Alt | rs137853342(A;A) |
Reference | Rs137853342(G;G) |
Significance | Pathogenic |
Disease | Pseudoprimary hyperaldosteronism |
Variation | info |
Gene | SCNN1G |
CLNDBN | Pseudoprimary hyperaldosteronism |
Reversed | 0 |
HGVS | NC_000016.9:g.23226558G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000009372.3, |