rs121908652
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs121908652(C;T) |
Make rs121908652(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 22129682 |
Gene | WNT4 |
is a | snp |
is | mentioned by |
dbSNP | rs121908652 |
dbSNP (classic) | rs121908652 |
ClinGen | rs121908652 |
ebi | rs121908652 |
HLI | rs121908652 |
Exac | rs121908652 |
Gnomad | rs121908652 |
Varsome | rs121908652 |
LitVar | rs121908652 |
Map | rs121908652 |
PheGenI | rs121908652 |
Biobank | rs121908652 |
1000 genomes | rs121908652 |
hgdp | rs121908652 |
ensembl | rs121908652 |
geneview | rs121908652 |
scholar | rs121908652 |
rs121908652 | |
pharmgkb | rs121908652 |
gwascentral | rs121908652 |
openSNP | rs121908652 |
23andMe | rs121908652 |
SNPshot | rs121908652 |
SNPdbe | rs121908652 |
MSV3d | rs121908652 |
GWAS Ctlg | rs121908652 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121908652(T;T) |
Alt | rs121908652(T;T) |
Reference | Rs121908652(C;C) |
Significance | Pathogenic |
Disease | Mullerian aplasia and hyperandrogenism |
Variation | info |
Gene | WNT4 |
CLNDBN | Mullerian aplasia and hyperandrogenism |
Reversed | 1 |
HGVS | NC_000001.10:g.22456175G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000006690.2, |