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rs182798226

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs182798226(A;A)
Make rs182798226(A;G)
Make rs182798226(G;G)
ReferenceGRCh38 38.1/142
Chromosome6
Position31271285
GeneHLA-C
is asnp
is mentioned by
dbSNPrs182798226
ebirs182798226
HLIrs182798226
Exacrs182798226
Varsomers182798226
Maprs182798226
PheGenIrs182798226
hapmaprs182798226
1000 genomesrs182798226
hgdprs182798226
ensemblrs182798226
gopubmedrs182798226
geneviewrs182798226
scholarrs182798226
googlers182798226
pharmgkbrs182798226
gwascentralrs182798226
openSNPrs182798226
23andMers182798226
23andMe allrs182798226
SNP Nexus

SNPshotrs182798226
SNPdbers182798226
MSV3drs182798226
GWAS Ctlgrs182798226
Max Magnitude0
ClinVar
Risk rs182798226(A,G;A,G)
Alt rs182798226(A,G;A,G)
Reference rs182798226(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31239062C>G
CLNSRC
CLNACC