rs79636386
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs79636386(A;A) |
Make rs79636386(A;G) |
Make rs79636386(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31271153 |
Gene | HLA-C |
is a | snp |
is | mentioned by |
dbSNP | rs79636386 |
dbSNP (classic) | rs79636386 |
ClinGen | rs79636386 |
ebi | rs79636386 |
HLI | rs79636386 |
Exac | rs79636386 |
Gnomad | rs79636386 |
Varsome | rs79636386 |
LitVar | rs79636386 |
Map | rs79636386 |
PheGenI | rs79636386 |
Biobank | rs79636386 |
1000 genomes | rs79636386 |
hgdp | rs79636386 |
ensembl | rs79636386 |
geneview | rs79636386 |
scholar | rs79636386 |
rs79636386 | |
pharmgkb | rs79636386 |
gwascentral | rs79636386 |
openSNP | rs79636386 |
23andMe | rs79636386 |
SNPshot | rs79636386 |
SNPdbe | rs79636386 |
MSV3d | rs79636386 |
GWAS Ctlg | rs79636386 |
GMAF | 0.3017 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs79636386(A;A) rs79636386(G;G) |
Alt | rs79636386(A;A) rs79636386(G;G) |
Reference | Rs79636386(T;T) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-C |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31238930A>C; NC_000006.11:g.31238930A>T |
CLNSRC | |
CLNACC |