rs17878838
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs17878838(A;A) |
Make rs17878838(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 29943567 |
Gene | HLA-A |
is a | snp |
is | mentioned by |
dbSNP | rs17878838 |
dbSNP (classic) | rs17878838 |
ClinGen | rs17878838 |
ebi | rs17878838 |
HLI | rs17878838 |
Exac | rs17878838 |
Gnomad | rs17878838 |
Varsome | rs17878838 |
LitVar | rs17878838 |
Map | rs17878838 |
PheGenI | rs17878838 |
Biobank | rs17878838 |
1000 genomes | rs17878838 |
hgdp | rs17878838 |
ensembl | rs17878838 |
geneview | rs17878838 |
scholar | rs17878838 |
rs17878838 | |
pharmgkb | rs17878838 |
gwascentral | rs17878838 |
openSNP | rs17878838 |
23andMe | rs17878838 |
SNPshot | rs17878838 |
SNPdbe | rs17878838 |
MSV3d | rs17878838 |
GWAS Ctlg | rs17878838 |
GMAF | 0.1524 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs17878838(A;A) rs17878838(T;T) |
Alt | rs17878838(A;A) rs17878838(T;T) |
Reference | Rs17878838(C;C) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-A |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.29911344C>A; NC_000006.11:g.29911344C>T |
CLNSRC | |
CLNACC |