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rs41561718

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41561718(-;-)
Make rs41561718(-;G)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324752
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41561718
ebirs41561718
HLIrs41561718
Exacrs41561718
Varsomers41561718
Maprs41561718
PheGenIrs41561718
hapmaprs41561718
1000 genomesrs41561718
hgdprs41561718
ensemblrs41561718
gopubmedrs41561718
geneviewrs41561718
scholarrs41561718
googlers41561718
pharmgkbrs41561718
gwascentralrs41561718
openSNPrs41561718
23andMers41561718
23andMe allrs41561718
SNP Nexus

SNPshotrs41561718
SNPdbers41561718
MSV3drs41561718
GWAS Ctlgrs41561718
StatusDeleted
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs41561718(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324752delC
CLNSRC
CLNACC