rs41563617
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs41563617(A;A) |
Make rs41563617(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 29943022 |
Gene | HLA-A |
is a | snp |
is | mentioned by |
dbSNP | rs41563617 |
dbSNP (classic) | rs41563617 |
ClinGen | rs41563617 |
ebi | rs41563617 |
HLI | rs41563617 |
Exac | rs41563617 |
Gnomad | rs41563617 |
Varsome | rs41563617 |
LitVar | rs41563617 |
Map | rs41563617 |
PheGenI | rs41563617 |
Biobank | rs41563617 |
1000 genomes | rs41563617 |
hgdp | rs41563617 |
ensembl | rs41563617 |
geneview | rs41563617 |
scholar | rs41563617 |
rs41563617 | |
pharmgkb | rs41563617 |
gwascentral | rs41563617 |
openSNP | rs41563617 |
23andMe | rs41563617 |
SNPshot | rs41563617 |
SNPdbe | rs41563617 |
MSV3d | rs41563617 |
GWAS Ctlg | rs41563617 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs41563617(A;A) |
Alt | rs41563617(A;A) |
Reference | Rs41563617(G;G) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-A |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.29910799G>A |
CLNSRC | |
CLNACC |