rs137853157
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs137853157(A;A) |
Make rs137853157(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 48251770 |
Gene | LOC107984758, SLC12A1 |
is a | snp |
is | mentioned by |
dbSNP | rs137853157 |
dbSNP (classic) | rs137853157 |
ClinGen | rs137853157 |
ebi | rs137853157 |
HLI | rs137853157 |
Exac | rs137853157 |
Gnomad | rs137853157 |
Varsome | rs137853157 |
LitVar | rs137853157 |
Map | rs137853157 |
PheGenI | rs137853157 |
Biobank | rs137853157 |
1000 genomes | rs137853157 |
hgdp | rs137853157 |
ensembl | rs137853157 |
geneview | rs137853157 |
scholar | rs137853157 |
rs137853157 | |
pharmgkb | rs137853157 |
gwascentral | rs137853157 |
openSNP | rs137853157 |
23andMe | rs137853157 |
SNPshot | rs137853157 |
SNPdbe | rs137853157 |
MSV3d | rs137853157 |
GWAS Ctlg | rs137853157 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs137853157(A;A) |
Alt | rs137853157(A;A) |
Reference | Rs137853157(G;G) |
Significance | Pathogenic |
Disease | Bartter syndrome |
Variation | info |
Gene | SLC12A1 |
CLNDBN | Bartter syndrome, type 1, antenatal |
Reversed | 0 |
HGVS | NC_000015.9:g.48543967G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000009295.3, |