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rs41563720

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41563720(-;-)
Make rs41563720(-;C)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324033
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41563720
ebirs41563720
HLIrs41563720
Exacrs41563720
Varsomers41563720
Maprs41563720
PheGenIrs41563720
hapmaprs41563720
1000 genomesrs41563720
hgdprs41563720
ensemblrs41563720
gopubmedrs41563720
geneviewrs41563720
scholarrs41563720
googlers41563720
pharmgkbrs41563720
gwascentralrs41563720
openSNPrs41563720
23andMers41563720
23andMe allrs41563720
SNP Nexus

SNPshotrs41563720
SNPdbers41563720
MSV3drs41563720
GWAS Ctlgrs41563720
StatusDeleted
Max Magnitude0
ClinVar
Risk rs41563720(;)
Alt rs41563720(;)
Reference rs41563720(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324033delG
CLNSRC
CLNACC