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rs3190923

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs3190923(C;C)
Make rs3190923(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356722
GeneHLA-B
is asnp
is mentioned by
dbSNPrs3190923
ebirs3190923
HLIrs3190923
Exacrs3190923
Varsomers3190923
Maprs3190923
PheGenIrs3190923
hapmaprs3190923
1000 genomesrs3190923
hgdprs3190923
ensemblrs3190923
gopubmedrs3190923
geneviewrs3190923
scholarrs3190923
googlers3190923
pharmgkbrs3190923
gwascentralrs3190923
openSNPrs3190923
23andMers3190923
23andMe allrs3190923
SNP Nexus

SNPshotrs3190923
SNPdbers3190923
MSV3drs3190923
GWAS Ctlgrs3190923
Max Magnitude0
ClinVar
Risk rs3190923(C;C)
Alt rs3190923(C;C)
Reference rs3190923(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324499C>G
CLNSRC
CLNACC