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rs41562017

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41562017(A;A)
Make rs41562017(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356341
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41562017
ebirs41562017
HLIrs41562017
Exacrs41562017
Varsomers41562017
Maprs41562017
PheGenIrs41562017
hapmaprs41562017
1000 genomesrs41562017
hgdprs41562017
ensemblrs41562017
gopubmedrs41562017
geneviewrs41562017
scholarrs41562017
googlers41562017
pharmgkbrs41562017
gwascentralrs41562017
openSNPrs41562017
23andMers41562017
23andMe allrs41562017
SNP Nexus

SNPshotrs41562017
SNPdbers41562017
MSV3drs41562017
GWAS Ctlgrs41562017
Max Magnitude0
ClinVar
Risk rs41562017(A,T;A,T)
Alt rs41562017(A,T;A,T)
Reference rs41562017(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324118C>A; NC_000006.11:g.31324118C>T
CLNSRC
CLNACC