rs17879162
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs17879162(A;A) |
Make rs17879162(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31269480 |
Gene | HLA-C |
is a | snp |
is | mentioned by |
dbSNP | rs17879162 |
dbSNP (classic) | rs17879162 |
ClinGen | rs17879162 |
ebi | rs17879162 |
HLI | rs17879162 |
Exac | rs17879162 |
Gnomad | rs17879162 |
Varsome | rs17879162 |
LitVar | rs17879162 |
Map | rs17879162 |
PheGenI | rs17879162 |
Biobank | rs17879162 |
1000 genomes | rs17879162 |
hgdp | rs17879162 |
ensembl | rs17879162 |
geneview | rs17879162 |
scholar | rs17879162 |
rs17879162 | |
pharmgkb | rs17879162 |
gwascentral | rs17879162 |
openSNP | rs17879162 |
23andMe | rs17879162 |
SNPshot | rs17879162 |
SNPdbe | rs17879162 |
MSV3d | rs17879162 |
GWAS Ctlg | rs17879162 |
GMAF | 0.05005 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs17879162(A;A) |
Alt | rs17879162(A;A) |
Reference | Rs17879162(G;G) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-C |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31237257C>T |
CLNSRC | |
CLNACC |