rs41558913
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs41558913(A;A) |
Make rs41558913(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 29943488 |
Gene | HLA-A |
is a | snp |
is | mentioned by |
dbSNP | rs41558913 |
dbSNP (classic) | rs41558913 |
ClinGen | rs41558913 |
ebi | rs41558913 |
HLI | rs41558913 |
Exac | rs41558913 |
Gnomad | rs41558913 |
Varsome | rs41558913 |
LitVar | rs41558913 |
Map | rs41558913 |
PheGenI | rs41558913 |
Biobank | rs41558913 |
1000 genomes | rs41558913 |
hgdp | rs41558913 |
ensembl | rs41558913 |
geneview | rs41558913 |
scholar | rs41558913 |
rs41558913 | |
pharmgkb | rs41558913 |
gwascentral | rs41558913 |
openSNP | rs41558913 |
23andMe | rs41558913 |
SNPshot | rs41558913 |
SNPdbe | rs41558913 |
MSV3d | rs41558913 |
GWAS Ctlg | rs41558913 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs41558913(A;A) rs41558913(G;G) rs41558913(T;T) |
Alt | rs41558913(A;A) rs41558913(G;G) rs41558913(T;T) |
Reference | Rs41558913(C;C) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-A |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.29911265C>A; NC_000006.11:g.29911265C>G; NC_000006.11:g.29911265C>T |
CLNSRC | |
CLNACC |