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rs1071649

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1071649(A;A)
Make rs1071649(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271337
GeneHLA-C
is asnp
is mentioned by
dbSNPrs1071649
ebirs1071649
HLIrs1071649
Exacrs1071649
Varsomers1071649
Maprs1071649
PheGenIrs1071649
hapmaprs1071649
1000 genomesrs1071649
hgdprs1071649
ensemblrs1071649
gopubmedrs1071649
geneviewrs1071649
scholarrs1071649
googlers1071649
pharmgkbrs1071649
gwascentralrs1071649
openSNPrs1071649
23andMers1071649
23andMe allrs1071649
SNP Nexus

SNPshotrs1071649
SNPdbers1071649
MSV3drs1071649
GWAS Ctlgrs1071649
GMAF0.2043
Max Magnitude0
ClinVar
Risk rs1071649(A,T;A,T)
Alt rs1071649(A,T;A,T)
Reference rs1071649(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239114G>A; NC_000006.11:g.31239114G>T
CLNSRC
CLNACC