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rs66620546

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs66620546(C;G)
Make rs66620546(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269686
GeneHLA-C
is asnp
is mentioned by
dbSNPrs66620546
ebirs66620546
HLIrs66620546
Exacrs66620546
Varsomers66620546
Maprs66620546
PheGenIrs66620546
hapmaprs66620546
1000 genomesrs66620546
hgdprs66620546
ensemblrs66620546
gopubmedrs66620546
geneviewrs66620546
scholarrs66620546
googlers66620546
pharmgkbrs66620546
gwascentralrs66620546
openSNPrs66620546
23andMers66620546
23andMe allrs66620546
SNP Nexus

SNPshotrs66620546
SNPdbers66620546
MSV3drs66620546
GWAS Ctlgrs66620546
GMAF0.2204
Max Magnitude0
ClinVar
Risk rs66620546(G;G)
Alt rs66620546(G;G)
Reference rs66620546(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31237463C>G
CLNSRC
CLNACC