rs151344502
From SNPedia
Merged into | rs111647200 |
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs151344502(A;A) |
Make rs151344502(A;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 32039807 |
Gene | CYP21A2 |
is a | snp |
is | mentioned by |
dbSNP | rs151344502 |
dbSNP (classic) | rs151344502 |
ClinGen | rs151344502 |
ebi | rs151344502 |
HLI | rs151344502 |
Exac | rs151344502 |
Gnomad | rs151344502 |
Varsome | rs151344502 |
LitVar | rs151344502 |
Map | rs151344502 |
PheGenI | rs151344502 |
Biobank | rs151344502 |
1000 genomes | rs151344502 |
hgdp | rs151344502 |
ensembl | rs151344502 |
geneview | rs151344502 |
scholar | rs151344502 |
rs151344502 | |
pharmgkb | rs151344502 |
gwascentral | rs151344502 |
openSNP | rs151344502 |
23andMe | rs151344502 |
SNPshot | rs151344502 |
SNPdbe | rs151344502 |
MSV3d | rs151344502 |
GWAS Ctlg | rs151344502 |
Status | Merged into rs111647200 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs151344502(A;A) |
Alt | rs151344502(A;A) |
Reference | Rs151344502(T;T) |
Significance | Probable-Pathogenic |
Disease | |
Variation | info |
Gene | CYP21A2 |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.32007584T>A |
CLNSRC | |
CLNACC |