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rs142964417

From SNPedia

Merged intors1050370
Orientationminus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs142964417(A;A)
Make rs142964417(A;C)
Make rs142964417(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356312
GeneHLA-B
is asnp
is mentioned by
dbSNPrs142964417
ebirs142964417
HLIrs142964417
Exacrs142964417
Varsomers142964417
Maprs142964417
PheGenIrs142964417
hapmaprs142964417
1000 genomesrs142964417
hgdprs142964417
ensemblrs142964417
gopubmedrs142964417
geneviewrs142964417
scholarrs142964417
googlers142964417
pharmgkbrs142964417
gwascentralrs142964417
openSNPrs142964417
23andMers142964417
23andMe allrs142964417
SNP Nexus

SNPshotrs142964417
SNPdbers142964417
MSV3drs142964417
GWAS Ctlgrs142964417
StatusMerged into rs1050370
Max Magnitude0
ClinVar
Risk rs142964417(A;A)
Alt rs142964417(A;A)
Reference rs142964417(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31324089G>A
CLNSRC
CLNACC