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rs17192932

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs17192932(C;G)
Make rs17192932(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354352
GeneHLA-B
is asnp
is mentioned by
dbSNPrs17192932
ebirs17192932
HLIrs17192932
Exacrs17192932
Varsomers17192932
Maprs17192932
PheGenIrs17192932
hapmaprs17192932
1000 genomesrs17192932
hgdprs17192932
ensemblrs17192932
gopubmedrs17192932
geneviewrs17192932
scholarrs17192932
googlers17192932
pharmgkbrs17192932
gwascentralrs17192932
openSNPrs17192932
23andMers17192932
23andMe allrs17192932
SNP Nexus

SNPshotrs17192932
SNPdbers17192932
MSV3drs17192932
GWAS Ctlgrs17192932
GMAF0.05739
Max Magnitude0
ClinVar
Risk rs17192932(G;G)
Alt rs17192932(G;G)
Reference rs17192932(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31322129C>G
CLNSRC
CLNACC