rs12697943
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs12697943(G;T) |
Make rs12697943(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31356280 |
Gene | HLA-B, MIR6891 |
is a | snp |
is | mentioned by |
dbSNP | rs12697943 |
dbSNP (classic) | rs12697943 |
ClinGen | rs12697943 |
ebi | rs12697943 |
HLI | rs12697943 |
Exac | rs12697943 |
Gnomad | rs12697943 |
Varsome | rs12697943 |
LitVar | rs12697943 |
Map | rs12697943 |
PheGenI | rs12697943 |
Biobank | rs12697943 |
1000 genomes | rs12697943 |
hgdp | rs12697943 |
ensembl | rs12697943 |
geneview | rs12697943 |
scholar | rs12697943 |
rs12697943 | |
pharmgkb | rs12697943 |
gwascentral | rs12697943 |
openSNP | rs12697943 |
23andMe | rs12697943 |
SNPshot | rs12697943 |
SNPdbe | rs12697943 |
MSV3d | rs12697943 |
GWAS Ctlg | rs12697943 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs12697943(A;A) rs12697943(C;C) rs12697943(T;T) |
Alt | rs12697943(A;A) rs12697943(C;C) rs12697943(T;T) |
Reference | Rs12697943(G;G) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31324057C>A; NC_000006.11:g.31324057C>G; NC_000006.11:g.31324057C>T |
CLNSRC | |
CLNACC |