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rs2308598

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs2308598(A;G)
Make rs2308598(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271112
GeneHLA-C
is asnp
is mentioned by
dbSNPrs2308598
ebirs2308598
HLIrs2308598
Exacrs2308598
Varsomers2308598
Maprs2308598
PheGenIrs2308598
hapmaprs2308598
1000 genomesrs2308598
hgdprs2308598
ensemblrs2308598
gopubmedrs2308598
geneviewrs2308598
scholarrs2308598
googlers2308598
pharmgkbrs2308598
gwascentralrs2308598
openSNPrs2308598
23andMers2308598
23andMe allrs2308598
SNP Nexus

SNPshotrs2308598
SNPdbers2308598
MSV3drs2308598
GWAS Ctlgrs2308598
GMAF0.01928
Max Magnitude0
ClinVar
Risk rs2308598(C,G;C,G)
Alt rs2308598(C,G;C,G)
Reference rs2308598(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238889T>C
CLNSRC
CLNACC