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rs2308604

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs2308604(A;G)
Make rs2308604(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271074
GeneHLA-C
is asnp
is mentioned by
dbSNPrs2308604
dbSNP (classic)rs2308604
ClinGenrs2308604
ebirs2308604
HLIrs2308604
Exacrs2308604
Gnomadrs2308604
Varsomers2308604
LitVarrs2308604
Maprs2308604
PheGenIrs2308604
Biobankrs2308604
1000 genomesrs2308604
hgdprs2308604
ensemblrs2308604
geneviewrs2308604
scholarrs2308604
googlers2308604
pharmgkbrs2308604
gwascentralrs2308604
openSNPrs2308604
23andMers2308604
SNPshotrs2308604
SNPdbers2308604
MSV3drs2308604
GWAS Ctlgrs2308604
GMAF0.2112
Max Magnitude0
ClinVar
Risk rs2308604(G;G) rs2308604(T;T)
Alt rs2308604(G;G) rs2308604(T;T)
Reference Rs2308604(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238851T>A; NC_000006.11:g.31238851T>C
CLNSRC
CLNACC