rs41546314
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs41546314(C;T) |
Make rs41546314(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 29942601 |
Gene | HLA-A |
is a | snp |
is | mentioned by |
dbSNP | rs41546314 |
dbSNP (classic) | rs41546314 |
ClinGen | rs41546314 |
ebi | rs41546314 |
HLI | rs41546314 |
Exac | rs41546314 |
Gnomad | rs41546314 |
Varsome | rs41546314 |
LitVar | rs41546314 |
Map | rs41546314 |
PheGenI | rs41546314 |
Biobank | rs41546314 |
1000 genomes | rs41546314 |
hgdp | rs41546314 |
ensembl | rs41546314 |
geneview | rs41546314 |
scholar | rs41546314 |
rs41546314 | |
pharmgkb | rs41546314 |
gwascentral | rs41546314 |
openSNP | rs41546314 |
23andMe | rs41546314 |
SNPshot | rs41546314 |
SNPdbe | rs41546314 |
MSV3d | rs41546314 |
GWAS Ctlg | rs41546314 |
GMAF | 0.2663 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs41546314(T;T) |
Alt | rs41546314(T;T) |
Reference | Rs41546314(C;C) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-A |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.29910378C>T |
CLNSRC | |
CLNACC |