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rs41547815

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41547815(A;A)
Make rs41547815(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356260
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41547815
ebirs41547815
HLIrs41547815
Exacrs41547815
Varsomers41547815
Maprs41547815
PheGenIrs41547815
hapmaprs41547815
1000 genomesrs41547815
hgdprs41547815
ensemblrs41547815
gopubmedrs41547815
geneviewrs41547815
scholarrs41547815
googlers41547815
pharmgkbrs41547815
gwascentralrs41547815
openSNPrs41547815
23andMers41547815
23andMe allrs41547815
SNP Nexus

SNPshotrs41547815
SNPdbers41547815
MSV3drs41547815
GWAS Ctlgrs41547815
Max Magnitude0
ClinVar
Risk rs41547815(A,C;A,C)
Alt rs41547815(A,C;A,C)
Reference rs41547815(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324037C>G; NC_000006.11:g.31324037C>T
CLNSRC
CLNACC