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rs4999716

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs4999716(A;A)
Make rs4999716(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356450
GeneHLA-B
is asnp
is mentioned by
dbSNPrs4999716
ebirs4999716
HLIrs4999716
Exacrs4999716
Varsomers4999716
Maprs4999716
PheGenIrs4999716
hapmaprs4999716
1000 genomesrs4999716
hgdprs4999716
ensemblrs4999716
gopubmedrs4999716
geneviewrs4999716
scholarrs4999716
googlers4999716
pharmgkbrs4999716
gwascentralrs4999716
openSNPrs4999716
23andMers4999716
23andMe allrs4999716
SNP Nexus

SNPshotrs4999716
SNPdbers4999716
MSV3drs4999716
GWAS Ctlgrs4999716
GMAF0.1368
Max Magnitude0
ClinVar
Risk rs4999716(A;A)
Alt rs4999716(A;A)
Reference rs4999716(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31324227C>A
CLNSRC
CLNACC