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rs2308628

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2308628(A;A)
Make rs2308628(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270214
GeneHLA-C
is asnp
is mentioned by
dbSNPrs2308628
ebirs2308628
HLIrs2308628
Exacrs2308628
Varsomers2308628
Maprs2308628
PheGenIrs2308628
hapmaprs2308628
1000 genomesrs2308628
hgdprs2308628
ensemblrs2308628
gopubmedrs2308628
geneviewrs2308628
scholarrs2308628
googlers2308628
pharmgkbrs2308628
gwascentralrs2308628
openSNPrs2308628
23andMers2308628
23andMe allrs2308628
SNP Nexus

SNPshotrs2308628
SNPdbers2308628
MSV3drs2308628
GWAS Ctlgrs2308628
GMAF0.4082
Max Magnitude0
ClinVar
Risk rs2308628(A;A)
Alt rs2308628(A;A)
Reference rs2308628(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237991G>T
CLNSRC
CLNACC