rs45617033
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs45617033(C;T) |
Make rs45617033(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 29942800 |
Gene | HLA-A |
is a | snp |
is | mentioned by |
dbSNP | rs45617033 |
dbSNP (classic) | rs45617033 |
ClinGen | rs45617033 |
ebi | rs45617033 |
HLI | rs45617033 |
Exac | rs45617033 |
Gnomad | rs45617033 |
Varsome | rs45617033 |
LitVar | rs45617033 |
Map | rs45617033 |
PheGenI | rs45617033 |
Biobank | rs45617033 |
1000 genomes | rs45617033 |
hgdp | rs45617033 |
ensembl | rs45617033 |
geneview | rs45617033 |
scholar | rs45617033 |
rs45617033 | |
pharmgkb | rs45617033 |
gwascentral | rs45617033 |
openSNP | rs45617033 |
23andMe | rs45617033 |
SNPshot | rs45617033 |
SNPdbe | rs45617033 |
MSV3d | rs45617033 |
GWAS Ctlg | rs45617033 |
GMAF | 0.02938 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs45617033(G;G) rs45617033(T;T) |
Alt | rs45617033(G;G) rs45617033(T;T) |
Reference | Rs45617033(C;C) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-A |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.29910577C>G; NC_000006.11:g.29910577C>T |
CLNSRC | |
CLNACC |