Have questions? Visit https://www.reddit.com/r/SNPedia

rs147324178

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs147324178(C;C)
Make rs147324178(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356965
GeneHLA-B
is asnp
is mentioned by
dbSNPrs147324178
ebirs147324178
HLIrs147324178
Exacrs147324178
Varsomers147324178
Maprs147324178
PheGenIrs147324178
hapmaprs147324178
1000 genomesrs147324178
hgdprs147324178
ensemblrs147324178
gopubmedrs147324178
geneviewrs147324178
scholarrs147324178
googlers147324178
pharmgkbrs147324178
gwascentralrs147324178
openSNPrs147324178
23andMers147324178
23andMe allrs147324178
SNP Nexus

SNPshotrs147324178
SNPdbers147324178
MSV3drs147324178
GWAS Ctlgrs147324178
GMAF0.1694
Max Magnitude0
ClinVar
Risk rs147324178(A,C,G;A,C,G)
Alt rs147324178(A,C,G;A,C,G)
Reference rs147324178(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31324742T>C
CLNSRC
CLNACC