rs137852574
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs137852574(G;G) |
Make rs137852574(G;T) |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 67723688 |
Gene | AR |
is a | snp |
is | mentioned by |
dbSNP | rs137852574 |
dbSNP (classic) | rs137852574 |
ClinGen | rs137852574 |
ebi | rs137852574 |
HLI | rs137852574 |
Exac | rs137852574 |
Gnomad | rs137852574 |
Varsome | rs137852574 |
LitVar | rs137852574 |
Map | rs137852574 |
PheGenI | rs137852574 |
Biobank | rs137852574 |
1000 genomes | rs137852574 |
hgdp | rs137852574 |
ensembl | rs137852574 |
geneview | rs137852574 |
scholar | rs137852574 |
rs137852574 | |
pharmgkb | rs137852574 |
gwascentral | rs137852574 |
openSNP | rs137852574 |
23andMe | rs137852574 |
SNPshot | rs137852574 |
SNPdbe | rs137852574 |
MSV3d | rs137852574 |
GWAS Ctlg | rs137852574 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs137852574(G;G) |
Alt | rs137852574(G;G) |
Reference | Rs137852574(T;T) |
Significance | Pathogenic |
Disease | Hypospadias 1 |
Variation | info |
Gene | AR |
CLNDBN | Hypospadias 1, X-linked |
Reversed | 0 |
HGVS | NC_000023.10:g.66943530T>G |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000010498.3, |