rs2276447
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs2276447(C;T) |
Make rs2276447(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 29944427 |
Gene | HLA-A |
is a | snp |
is | mentioned by |
dbSNP | rs2276447 |
dbSNP (classic) | rs2276447 |
ClinGen | rs2276447 |
ebi | rs2276447 |
HLI | rs2276447 |
Exac | rs2276447 |
Gnomad | rs2276447 |
Varsome | rs2276447 |
LitVar | rs2276447 |
Map | rs2276447 |
PheGenI | rs2276447 |
Biobank | rs2276447 |
1000 genomes | rs2276447 |
hgdp | rs2276447 |
ensembl | rs2276447 |
geneview | rs2276447 |
scholar | rs2276447 |
rs2276447 | |
pharmgkb | rs2276447 |
gwascentral | rs2276447 |
openSNP | rs2276447 |
23andMe | rs2276447 |
SNPshot | rs2276447 |
SNPdbe | rs2276447 |
MSV3d | rs2276447 |
GWAS Ctlg | rs2276447 |
GMAF | 0.4656 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs2276447(G;G) rs2276447(T;T) |
Alt | rs2276447(G;G) rs2276447(T;T) |
Reference | Rs2276447(C;C) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-A |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.29912204C>T |
CLNSRC | |
CLNACC |