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rs2308618

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2308618(C;T)
Make rs2308618(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270349
GeneHLA-C
is asnp
is mentioned by
dbSNPrs2308618
ebirs2308618
HLIrs2308618
Exacrs2308618
Varsomers2308618
Maprs2308618
PheGenIrs2308618
hapmaprs2308618
1000 genomesrs2308618
hgdprs2308618
ensemblrs2308618
gopubmedrs2308618
geneviewrs2308618
scholarrs2308618
googlers2308618
pharmgkbrs2308618
gwascentralrs2308618
openSNPrs2308618
23andMers2308618
23andMe allrs2308618
SNP Nexus

SNPshotrs2308618
SNPdbers2308618
MSV3drs2308618
GWAS Ctlgrs2308618
GMAF0.1515
Max Magnitude0
ClinVar
Risk rs2308618(T;T)
Alt rs2308618(T;T)
Reference rs2308618(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238126G>A
CLNSRC
CLNACC