rs1085307685
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Chromosome | X |
Position | 67717552 |
Gene | AR |
is a | snp |
is | mentioned by |
dbSNP | rs1085307685 |
dbSNP (classic) | rs1085307685 |
ClinGen | rs1085307685 |
ebi | rs1085307685 |
HLI | rs1085307685 |
Exac | rs1085307685 |
Gnomad | rs1085307685 |
Varsome | rs1085307685 |
LitVar | rs1085307685 |
Map | rs1085307685 |
PheGenI | rs1085307685 |
Biobank | rs1085307685 |
1000 genomes | rs1085307685 |
hgdp | rs1085307685 |
ensembl | rs1085307685 |
geneview | rs1085307685 |
scholar | rs1085307685 |
rs1085307685 | |
pharmgkb | rs1085307685 |
gwascentral | rs1085307685 |
openSNP | rs1085307685 |
23andMe | rs1085307685 |
SNPshot | rs1085307685 |
SNPdbe | rs1085307685 |
MSV3d | rs1085307685 |
GWAS Ctlg | rs1085307685 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1085307685(G;G) |
Alt | rs1085307685(G;G) |
Reference | Rs1085307685(A;A) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | AR |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000023.10:g.66937394A>G |
CLNSRC | |
CLNACC | RCV000488944.1, |