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rs41562716

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41562716(A;A)
Make rs41562716(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356297
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41562716
ebirs41562716
HLIrs41562716
Exacrs41562716
Varsomers41562716
Maprs41562716
PheGenIrs41562716
hapmaprs41562716
1000 genomesrs41562716
hgdprs41562716
ensemblrs41562716
gopubmedrs41562716
geneviewrs41562716
scholarrs41562716
googlers41562716
pharmgkbrs41562716
gwascentralrs41562716
openSNPrs41562716
23andMers41562716
23andMe allrs41562716
SNP Nexus

SNPshotrs41562716
SNPdbers41562716
MSV3drs41562716
GWAS Ctlgrs41562716
Max Magnitude0
ClinVar
Risk rs41562716(A,C;A,C)
Alt rs41562716(A,C;A,C)
Reference rs41562716(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324074C>G; NC_000006.11:g.31324074C>T
CLNSRC
CLNACC