rs17884362
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs17884362(A;A) |
Make rs17884362(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31270140 |
Gene | HLA-C |
is a | snp |
is | mentioned by |
dbSNP | rs17884362 |
dbSNP (classic) | rs17884362 |
ClinGen | rs17884362 |
ebi | rs17884362 |
HLI | rs17884362 |
Exac | rs17884362 |
Gnomad | rs17884362 |
Varsome | rs17884362 |
LitVar | rs17884362 |
Map | rs17884362 |
PheGenI | rs17884362 |
Biobank | rs17884362 |
1000 genomes | rs17884362 |
hgdp | rs17884362 |
ensembl | rs17884362 |
geneview | rs17884362 |
scholar | rs17884362 |
rs17884362 | |
pharmgkb | rs17884362 |
gwascentral | rs17884362 |
openSNP | rs17884362 |
23andMe | rs17884362 |
SNPshot | rs17884362 |
SNPdbe | rs17884362 |
MSV3d | rs17884362 |
GWAS Ctlg | rs17884362 |
GMAF | 0.1442 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs17884362(A;A) |
Alt | rs17884362(A;A) |
Reference | Rs17884362(G;G) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-C |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31237917C>T |
CLNSRC | |
CLNACC |