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rs41547332

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41547332(A;A)
Make rs41547332(A;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356419
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41547332
ebirs41547332
HLIrs41547332
Exacrs41547332
Varsomers41547332
Maprs41547332
PheGenIrs41547332
hapmaprs41547332
1000 genomesrs41547332
hgdprs41547332
ensemblrs41547332
gopubmedrs41547332
geneviewrs41547332
scholarrs41547332
googlers41547332
pharmgkbrs41547332
gwascentralrs41547332
openSNPrs41547332
23andMers41547332
23andMe allrs41547332
SNP Nexus

SNPshotrs41547332
SNPdbers41547332
MSV3drs41547332
GWAS Ctlgrs41547332
Max Magnitude0
ClinVar
Risk rs41547332(A,C;A,C)
Alt rs41547332(A,C;A,C)
Reference rs41547332(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324196A>G; NC_000006.11:g.31324196A>T
CLNSRC
CLNACC