rs114343571
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs114343571(A;A) |
Make rs114343571(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31270788 |
Gene | HLA-C |
is a | snp |
is | mentioned by |
dbSNP | rs114343571 |
dbSNP (classic) | rs114343571 |
ClinGen | rs114343571 |
ebi | rs114343571 |
HLI | rs114343571 |
Exac | rs114343571 |
Gnomad | rs114343571 |
Varsome | rs114343571 |
LitVar | rs114343571 |
Map | rs114343571 |
PheGenI | rs114343571 |
Biobank | rs114343571 |
1000 genomes | rs114343571 |
hgdp | rs114343571 |
ensembl | rs114343571 |
geneview | rs114343571 |
scholar | rs114343571 |
rs114343571 | |
pharmgkb | rs114343571 |
gwascentral | rs114343571 |
openSNP | rs114343571 |
23andMe | rs114343571 |
SNPshot | rs114343571 |
SNPdbe | rs114343571 |
MSV3d | rs114343571 |
GWAS Ctlg | rs114343571 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs114343571(A;A) |
Alt | rs114343571(A;A) |
Reference | Rs114343571(G;G) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-C |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.31238565G>A |
CLNSRC | |
CLNACC |