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rs146911342

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs146911342(C;T)
Make rs146911342(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270002
GeneHLA-C
is asnp
is mentioned by
dbSNPrs146911342
ebirs146911342
HLIrs146911342
Exacrs146911342
Varsomers146911342
Maprs146911342
PheGenIrs146911342
hapmaprs146911342
1000 genomesrs146911342
hgdprs146911342
ensemblrs146911342
gopubmedrs146911342
geneviewrs146911342
scholarrs146911342
googlers146911342
pharmgkbrs146911342
gwascentralrs146911342
openSNPrs146911342
23andMers146911342
23andMe allrs146911342
SNP Nexus

SNPshotrs146911342
SNPdbers146911342
MSV3drs146911342
GWAS Ctlgrs146911342
GMAF0.1263
Max Magnitude0
ClinVar
Risk rs146911342(T;T)
Alt rs146911342(T;T)
Reference rs146911342(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31237779C>T
CLNSRC
CLNACC