rs2075684
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs2075684(A;G) |
Make rs2075684(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 29942781 |
Gene | HLA-A |
is a | snp |
is | mentioned by |
dbSNP | rs2075684 |
dbSNP (classic) | rs2075684 |
ClinGen | rs2075684 |
ebi | rs2075684 |
HLI | rs2075684 |
Exac | rs2075684 |
Gnomad | rs2075684 |
Varsome | rs2075684 |
LitVar | rs2075684 |
Map | rs2075684 |
PheGenI | rs2075684 |
Biobank | rs2075684 |
1000 genomes | rs2075684 |
hgdp | rs2075684 |
ensembl | rs2075684 |
geneview | rs2075684 |
scholar | rs2075684 |
rs2075684 | |
pharmgkb | rs2075684 |
gwascentral | rs2075684 |
openSNP | rs2075684 |
23andMe | rs2075684 |
SNPshot | rs2075684 |
SNPdbe | rs2075684 |
MSV3d | rs2075684 |
GWAS Ctlg | rs2075684 |
GMAF | 0.4495 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs2075684(G;G) rs2075684(T;T) |
Alt | rs2075684(G;G) rs2075684(T;T) |
Reference | Rs2075684(A;A) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-A |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.29910558T>A; NC_000006.11:g.29910558T>C |
CLNSRC | |
CLNACC |