rs41562119
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs41562119(C;G) |
Make rs41562119(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 29943007 |
Gene | HLA-A |
is a | snp |
is | mentioned by |
dbSNP | rs41562119 |
dbSNP (classic) | rs41562119 |
ClinGen | rs41562119 |
ebi | rs41562119 |
HLI | rs41562119 |
Exac | rs41562119 |
Gnomad | rs41562119 |
Varsome | rs41562119 |
LitVar | rs41562119 |
Map | rs41562119 |
PheGenI | rs41562119 |
Biobank | rs41562119 |
1000 genomes | rs41562119 |
hgdp | rs41562119 |
ensembl | rs41562119 |
geneview | rs41562119 |
scholar | rs41562119 |
rs41562119 | |
pharmgkb | rs41562119 |
gwascentral | rs41562119 |
openSNP | rs41562119 |
23andMe | rs41562119 |
SNPshot | rs41562119 |
SNPdbe | rs41562119 |
MSV3d | rs41562119 |
GWAS Ctlg | rs41562119 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs41562119(G;G) rs41562119(T;T) |
Alt | rs41562119(G;G) rs41562119(T;T) |
Reference | Rs41562119(C;C) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-A |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.29910784C>G; NC_000006.11:g.29910784C>T |
CLNSRC | |
CLNACC |