rs875989810
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs875989810(G;T) |
Make rs875989810(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 10 |
Position | 49528426 |
Gene | ERCC6 |
is a | snp |
is | mentioned by |
dbSNP | rs875989810 |
dbSNP (classic) | rs875989810 |
ClinGen | rs875989810 |
ebi | rs875989810 |
HLI | rs875989810 |
Exac | rs875989810 |
Gnomad | rs875989810 |
Varsome | rs875989810 |
LitVar | rs875989810 |
Map | rs875989810 |
PheGenI | rs875989810 |
Biobank | rs875989810 |
1000 genomes | rs875989810 |
hgdp | rs875989810 |
ensembl | rs875989810 |
geneview | rs875989810 |
scholar | rs875989810 |
rs875989810 | |
pharmgkb | rs875989810 |
gwascentral | rs875989810 |
openSNP | rs875989810 |
23andMe | rs875989810 |
SNPshot | rs875989810 |
SNPdbe | rs875989810 |
MSV3d | rs875989810 |
GWAS Ctlg | rs875989810 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs875989810(T;T) |
Alt | rs875989810(T;T) |
Reference | Rs875989810(G;G) |
Significance | Pathogenic |
Disease | Premature ovarian failure 11 |
Variation | info |
Gene | ERCC6 |
CLNDBN | Premature ovarian failure 11 |
Reversed | 1 |
HGVS | NC_000010.10:g.50736472C>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000211122.1, |