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rs2074497

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs2074497(A;G)
Make rs2074497(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269950
GeneHLA-C
is asnp
is mentioned by
dbSNPrs2074497
ebirs2074497
HLIrs2074497
Exacrs2074497
Varsomers2074497
Maprs2074497
PheGenIrs2074497
hapmaprs2074497
1000 genomesrs2074497
hgdprs2074497
ensemblrs2074497
gopubmedrs2074497
geneviewrs2074497
scholarrs2074497
googlers2074497
pharmgkbrs2074497
gwascentralrs2074497
openSNPrs2074497
23andMers2074497
23andMe allrs2074497
SNP Nexus

SNPshotrs2074497
SNPdbers2074497
MSV3drs2074497
GWAS Ctlgrs2074497
Max Magnitude0
ClinVar
Risk rs2074497(G;G)
Alt rs2074497(G;G)
Reference rs2074497(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237727T>C
CLNSRC
CLNACC