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rs41564115

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41564115(A;A)
Make rs41564115(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354574
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41564115
ebirs41564115
HLIrs41564115
Exacrs41564115
Varsomers41564115
Maprs41564115
PheGenIrs41564115
hapmaprs41564115
1000 genomesrs41564115
hgdprs41564115
ensemblrs41564115
gopubmedrs41564115
geneviewrs41564115
scholarrs41564115
googlers41564115
pharmgkbrs41564115
gwascentralrs41564115
openSNPrs41564115
23andMers41564115
23andMe allrs41564115
SNP Nexus

SNPshotrs41564115
SNPdbers41564115
MSV3drs41564115
GWAS Ctlgrs41564115
GMAF0.0009183
Max Magnitude0
ClinVar
Risk rs41564115(A;A)
Alt rs41564115(A;A)
Reference rs41564115(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322351G>T
CLNSRC
CLNACC