rs137853320
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs137853320(C;T) |
Make rs137853320(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 50916059 |
Gene | BMP15 |
is a | snp |
is | mentioned by |
dbSNP | rs137853320 |
dbSNP (classic) | rs137853320 |
ClinGen | rs137853320 |
ebi | rs137853320 |
HLI | rs137853320 |
Exac | rs137853320 |
Gnomad | rs137853320 |
Varsome | rs137853320 |
LitVar | rs137853320 |
Map | rs137853320 |
PheGenI | rs137853320 |
Biobank | rs137853320 |
1000 genomes | rs137853320 |
hgdp | rs137853320 |
ensembl | rs137853320 |
geneview | rs137853320 |
scholar | rs137853320 |
rs137853320 | |
pharmgkb | rs137853320 |
gwascentral | rs137853320 |
openSNP | rs137853320 |
23andMe | rs137853320 |
SNPshot | rs137853320 |
SNPdbe | rs137853320 |
MSV3d | rs137853320 |
GWAS Ctlg | rs137853320 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs137853320(T;T) |
Alt | rs137853320(T;T) |
Reference | Rs137853320(C;C) |
Significance | Pathogenic |
Disease | Premature ovarian failure 4 |
Variation | info |
Gene | BMP15 |
CLNDBN | Premature ovarian failure 4 |
Reversed | 0 |
HGVS | NC_000023.10:g.50659059C>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000012228.20, |