rs878854403
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs878854403(A;A) |
Make rs878854403(A;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 10 |
Position | 49516282 |
Gene | ERCC6, PGBD3 |
is a | snp |
is | mentioned by |
dbSNP | rs878854403 |
dbSNP (classic) | rs878854403 |
ClinGen | rs878854403 |
ebi | rs878854403 |
HLI | rs878854403 |
Exac | rs878854403 |
Gnomad | rs878854403 |
Varsome | rs878854403 |
LitVar | rs878854403 |
Map | rs878854403 |
PheGenI | rs878854403 |
Biobank | rs878854403 |
1000 genomes | rs878854403 |
hgdp | rs878854403 |
ensembl | rs878854403 |
geneview | rs878854403 |
scholar | rs878854403 |
rs878854403 | |
pharmgkb | rs878854403 |
gwascentral | rs878854403 |
openSNP | rs878854403 |
23andMe | rs878854403 |
SNPshot | rs878854403 |
SNPdbe | rs878854403 |
MSV3d | rs878854403 |
GWAS Ctlg | rs878854403 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs878854403(A;A) |
Alt | rs878854403(A;A) |
Reference | Rs878854403(G;G) |
Significance | Pathogenic |
Disease | Premature ovarian failure 11 |
Variation | info |
Gene | ERCC6 PGBD3 |
CLNDBN | Premature ovarian failure 11 |
Reversed | 1 |
HGVS | NC_000010.10:g.50724328C>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000211123.2, |