rs878853033
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs878853033(G;G) |
Make rs878853033(G;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | X |
Position | 67686045 |
Gene | AR |
is a | snp |
is | mentioned by |
dbSNP | rs878853033 |
dbSNP (classic) | rs878853033 |
ClinGen | rs878853033 |
ebi | rs878853033 |
HLI | rs878853033 |
Exac | rs878853033 |
Gnomad | rs878853033 |
Varsome | rs878853033 |
LitVar | rs878853033 |
Map | rs878853033 |
PheGenI | rs878853033 |
Biobank | rs878853033 |
1000 genomes | rs878853033 |
hgdp | rs878853033 |
ensembl | rs878853033 |
geneview | rs878853033 |
scholar | rs878853033 |
rs878853033 | |
pharmgkb | rs878853033 |
gwascentral | rs878853033 |
openSNP | rs878853033 |
23andMe | rs878853033 |
SNPshot | rs878853033 |
SNPdbe | rs878853033 |
MSV3d | rs878853033 |
GWAS Ctlg | rs878853033 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs878853033(G;G) |
Alt | rs878853033(G;G) |
Reference | Rs878853033(T;T) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | AR |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000023.10:g.66905887T>G |
CLNSRC | |
CLNACC | RCV000224290.1, |