rs41561714
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs41561714(A;A) |
Make rs41561714(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 29943317 |
Gene | HLA-A |
is a | snp |
is | mentioned by |
dbSNP | rs41561714 |
dbSNP (classic) | rs41561714 |
ClinGen | rs41561714 |
ebi | rs41561714 |
HLI | rs41561714 |
Exac | rs41561714 |
Gnomad | rs41561714 |
Varsome | rs41561714 |
LitVar | rs41561714 |
Map | rs41561714 |
PheGenI | rs41561714 |
Biobank | rs41561714 |
1000 genomes | rs41561714 |
hgdp | rs41561714 |
ensembl | rs41561714 |
geneview | rs41561714 |
scholar | rs41561714 |
rs41561714 | |
pharmgkb | rs41561714 |
gwascentral | rs41561714 |
openSNP | rs41561714 |
23andMe | rs41561714 |
SNPshot | rs41561714 |
SNPdbe | rs41561714 |
MSV3d | rs41561714 |
GWAS Ctlg | rs41561714 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs41561714(A;A) rs41561714(C;C) rs41561714(T;T) |
Alt | rs41561714(A;A) rs41561714(C;C) rs41561714(T;T) |
Reference | Rs41561714(G;G) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-A |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.29911094G>A; NC_000006.11:g.29911094G>C; NC_000006.11:g.29911094G>T |
CLNSRC | |
CLNACC |