rs12721829
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs12721829(A;A) |
Make rs12721829(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31356431 |
Gene | HLA-B, MIR6891 |
is a | snp |
is | mentioned by |
dbSNP | rs12721829 |
dbSNP (classic) | rs12721829 |
ClinGen | rs12721829 |
ebi | rs12721829 |
HLI | rs12721829 |
Exac | rs12721829 |
Gnomad | rs12721829 |
Varsome | rs12721829 |
LitVar | rs12721829 |
Map | rs12721829 |
PheGenI | rs12721829 |
Biobank | rs12721829 |
1000 genomes | rs12721829 |
hgdp | rs12721829 |
ensembl | rs12721829 |
geneview | rs12721829 |
scholar | rs12721829 |
rs12721829 | |
pharmgkb | rs12721829 |
gwascentral | rs12721829 |
openSNP | rs12721829 |
23andMe | rs12721829 |
SNPshot | rs12721829 |
SNPdbe | rs12721829 |
MSV3d | rs12721829 |
GWAS Ctlg | rs12721829 |
GMAF | 0.2534 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs12721829(A;A) rs12721829(G;G) rs12721829(T;T) |
Alt | rs12721829(A;A) rs12721829(G;G) rs12721829(T;T) |
Reference | Rs12721829(C;C) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31324208G>A; NC_000006.11:g.31324208G>C; NC_000006.11:g.31324208G>T |
CLNSRC | |
CLNACC |