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rs2308567

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs2308567(C;C)
Make rs2308567(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271330
GeneHLA-C
is asnp
is mentioned by
dbSNPrs2308567
ebirs2308567
HLIrs2308567
Exacrs2308567
Varsomers2308567
Maprs2308567
PheGenIrs2308567
hapmaprs2308567
1000 genomesrs2308567
hgdprs2308567
ensemblrs2308567
gopubmedrs2308567
geneviewrs2308567
scholarrs2308567
googlers2308567
pharmgkbrs2308567
gwascentralrs2308567
openSNPrs2308567
23andMers2308567
23andMe allrs2308567
SNP Nexus

SNPshotrs2308567
SNPdbers2308567
MSV3drs2308567
GWAS Ctlgrs2308567
Max Magnitude0
ClinVar
Risk rs2308567(A,C,T;A,C,T)
Alt rs2308567(A,C,T;A,C,T)
Reference rs2308567(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239107C>A; NC_000006.11:g.31239107C>T
CLNSRC
CLNACC