rs3823342
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs3823342(C;C) |
Make rs3823342(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 29945290 |
Gene | HLA-A |
is a | snp |
is | mentioned by |
dbSNP | rs3823342 |
dbSNP (classic) | rs3823342 |
ClinGen | rs3823342 |
ebi | rs3823342 |
HLI | rs3823342 |
Exac | rs3823342 |
Gnomad | rs3823342 |
Varsome | rs3823342 |
LitVar | rs3823342 |
Map | rs3823342 |
PheGenI | rs3823342 |
Biobank | rs3823342 |
1000 genomes | rs3823342 |
hgdp | rs3823342 |
ensembl | rs3823342 |
geneview | rs3823342 |
scholar | rs3823342 |
rs3823342 | |
pharmgkb | rs3823342 |
gwascentral | rs3823342 |
openSNP | rs3823342 |
23andMe | rs3823342 |
SNPshot | rs3823342 |
SNPdbe | rs3823342 |
MSV3d | rs3823342 |
GWAS Ctlg | rs3823342 |
GMAF | 0.4743 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
ClinVar | |
---|---|
Risk | rs3823342(C;C) |
Alt | rs3823342(C;C) |
Reference | Rs3823342(T;T) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-A |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.29913067T>C |
CLNSRC | |
CLNACC |