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rs4999717

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs4999717(C;T)
Make rs4999717(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356571
GeneHLA-B
is asnp
is mentioned by
dbSNPrs4999717
ebirs4999717
HLIrs4999717
Exacrs4999717
Varsomers4999717
Maprs4999717
PheGenIrs4999717
hapmaprs4999717
1000 genomesrs4999717
hgdprs4999717
ensemblrs4999717
gopubmedrs4999717
geneviewrs4999717
scholarrs4999717
googlers4999717
pharmgkbrs4999717
gwascentralrs4999717
openSNPrs4999717
23andMers4999717
23andMe allrs4999717
SNP Nexus

SNPshotrs4999717
SNPdbers4999717
MSV3drs4999717
GWAS Ctlgrs4999717
GMAF0.1093
Max Magnitude0
ClinVar
Risk rs4999717(T;T)
Alt rs4999717(T;T)
Reference rs4999717(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31324348C>T
CLNSRC
CLNACC