rs78691935
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs78691935(A;A) |
Make rs78691935(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 29943434 |
Gene | HLA-A |
is a | snp |
is | mentioned by |
dbSNP | rs78691935 |
dbSNP (classic) | rs78691935 |
ClinGen | rs78691935 |
ebi | rs78691935 |
HLI | rs78691935 |
Exac | rs78691935 |
Gnomad | rs78691935 |
Varsome | rs78691935 |
LitVar | rs78691935 |
Map | rs78691935 |
PheGenI | rs78691935 |
Biobank | rs78691935 |
1000 genomes | rs78691935 |
hgdp | rs78691935 |
ensembl | rs78691935 |
geneview | rs78691935 |
scholar | rs78691935 |
rs78691935 | |
pharmgkb | rs78691935 |
gwascentral | rs78691935 |
openSNP | rs78691935 |
23andMe | rs78691935 |
SNPshot | rs78691935 |
SNPdbe | rs78691935 |
MSV3d | rs78691935 |
GWAS Ctlg | rs78691935 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs78691935(A;A) rs78691935(C;C) |
Alt | rs78691935(A;A) rs78691935(C;C) |
Reference | Rs78691935(G;G) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-A |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.29911211G>A; NC_000006.11:g.29911211G>C |
CLNSRC | |
CLNACC |