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rs3132688

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs3132688(C;C)
Make rs3132688(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942306
GeneHLA-A
is asnp
is mentioned by
dbSNPrs3132688
ebirs3132688
HLIrs3132688
Exacrs3132688
Varsomers3132688
Maprs3132688
PheGenIrs3132688
hapmaprs3132688
1000 genomesrs3132688
hgdprs3132688
ensemblrs3132688
gopubmedrs3132688
geneviewrs3132688
scholarrs3132688
googlers3132688
pharmgkbrs3132688
gwascentralrs3132688
openSNPrs3132688
23andMers3132688
23andMe allrs3132688
SNP Nexus

SNPshotrs3132688
SNPdbers3132688
MSV3drs3132688
GWAS Ctlgrs3132688
GMAF0.101
Max Magnitude0
ClinVar
Risk rs3132688(C;C)
Alt rs3132688(C;C)
Reference rs3132688(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 1
HGVS NC_000006.11:g.29910083A; NC_000006.11:g.29910083A>G
CLNSRC
CLNACC