rs875989885
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs875989885(C;T) |
Make rs875989885(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 10 |
Position | 133555706 |
Gene | SYCE1 |
is a | snp |
is | mentioned by |
dbSNP | rs875989885 |
dbSNP (classic) | rs875989885 |
ClinGen | rs875989885 |
ebi | rs875989885 |
HLI | rs875989885 |
Exac | rs875989885 |
Gnomad | rs875989885 |
Varsome | rs875989885 |
LitVar | rs875989885 |
Map | rs875989885 |
PheGenI | rs875989885 |
Biobank | rs875989885 |
1000 genomes | rs875989885 |
hgdp | rs875989885 |
ensembl | rs875989885 |
geneview | rs875989885 |
scholar | rs875989885 |
rs875989885 | |
pharmgkb | rs875989885 |
gwascentral | rs875989885 |
openSNP | rs875989885 |
23andMe | rs875989885 |
SNPshot | rs875989885 |
SNPdbe | rs875989885 |
MSV3d | rs875989885 |
GWAS Ctlg | rs875989885 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs875989885(T;T) |
Alt | rs875989885(T;T) |
Reference | Rs875989885(C;C) |
Significance | Pathogenic |
Disease | Premature ovarian failure 12 |
Variation | info |
Gene | SYCE1 |
CLNDBN | Premature ovarian failure 12 |
Reversed | 1 |
HGVS | NC_000010.10:g.135369210G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000211464.1, |