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rs41560718

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41560718(G;G)
Make rs41560718(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356494
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41560718
ebirs41560718
HLIrs41560718
Exacrs41560718
Varsomers41560718
Maprs41560718
PheGenIrs41560718
hapmaprs41560718
1000 genomesrs41560718
hgdprs41560718
ensemblrs41560718
gopubmedrs41560718
geneviewrs41560718
scholarrs41560718
googlers41560718
pharmgkbrs41560718
gwascentralrs41560718
openSNPrs41560718
23andMers41560718
23andMe allrs41560718
SNP Nexus

SNPshotrs41560718
SNPdbers41560718
MSV3drs41560718
GWAS Ctlgrs41560718
GMAF0.009642
Max Magnitude0
ClinVar
Risk rs41560718(G;G)
Alt rs41560718(G;G)
Reference rs41560718(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324271A>C
CLNSRC
CLNACC