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rs1065406

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1065406(A;A)
Make rs1065406(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271272
GeneHLA-C
is asnp
is mentioned by
dbSNPrs1065406
ebirs1065406
HLIrs1065406
Exacrs1065406
Varsomers1065406
Maprs1065406
PheGenIrs1065406
hapmaprs1065406
1000 genomesrs1065406
hgdprs1065406
ensemblrs1065406
gopubmedrs1065406
geneviewrs1065406
scholarrs1065406
googlers1065406
pharmgkbrs1065406
gwascentralrs1065406
openSNPrs1065406
23andMers1065406
23andMe allrs1065406
SNP Nexus

SNPshotrs1065406
SNPdbers1065406
MSV3drs1065406
GWAS Ctlgrs1065406
GMAF0.06887
Max Magnitude0
ClinVar
Risk rs1065406(A,G,T;A,G,T)
Alt rs1065406(A,G,T;A,G,T)
Reference rs1065406(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239049G>A; NC_000006.11:g.31239049G>C; NC_000006.11:g.31239049G>T
CLNSRC
CLNACC