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

rs45577931

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs45577931(A;A)
Make rs45577931(A;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355995
GeneHLA-B
is asnp
is mentioned by
dbSNPrs45577931
ebirs45577931
HLIrs45577931
Exacrs45577931
Varsomers45577931
Maprs45577931
PheGenIrs45577931
hapmaprs45577931
1000 genomesrs45577931
hgdprs45577931
ensemblrs45577931
gopubmedrs45577931
geneviewrs45577931
scholarrs45577931
googlers45577931
pharmgkbrs45577931
gwascentralrs45577931
openSNPrs45577931
23andMers45577931
23andMe allrs45577931
SNP Nexus

SNPshotrs45577931
SNPdbers45577931
MSV3drs45577931
GWAS Ctlgrs45577931
Max Magnitude0
ClinVar
Risk rs45577931(A;A)
Alt rs45577931(A;A)
Reference rs45577931(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323772A>T
CLNSRC
CLNACC