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rs41547422

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41547422(A;A)
Make rs41547422(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356192
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41547422
ebirs41547422
HLIrs41547422
Exacrs41547422
Varsomers41547422
Maprs41547422
PheGenIrs41547422
hapmaprs41547422
1000 genomesrs41547422
hgdprs41547422
ensemblrs41547422
gopubmedrs41547422
geneviewrs41547422
scholarrs41547422
googlers41547422
pharmgkbrs41547422
gwascentralrs41547422
openSNPrs41547422
23andMers41547422
23andMe allrs41547422
SNP Nexus

SNPshotrs41547422
SNPdbers41547422
MSV3drs41547422
GWAS Ctlgrs41547422
Max Magnitude0
ClinVar
Risk rs41547422(A,G,T;A,G,T)
Alt rs41547422(A,G,T;A,G,T)
Reference rs41547422(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323969G>A; NC_000006.11:g.31323969G>C; NC_000006.11:g.31323969G>T
CLNSRC
CLNACC