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rs41543415

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41543415(C;C)
Make rs41543415(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356743
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41543415
ebirs41543415
HLIrs41543415
Exacrs41543415
Varsomers41543415
Maprs41543415
PheGenIrs41543415
hapmaprs41543415
1000 genomesrs41543415
hgdprs41543415
ensemblrs41543415
gopubmedrs41543415
geneviewrs41543415
scholarrs41543415
googlers41543415
pharmgkbrs41543415
gwascentralrs41543415
openSNPrs41543415
23andMers41543415
23andMe allrs41543415
SNP Nexus

SNPshotrs41543415
SNPdbers41543415
MSV3drs41543415
GWAS Ctlgrs41543415
Max Magnitude0
ClinVar
Risk rs41543415(A,C,T;A,C,T)
Alt rs41543415(A,C,T;A,C,T)
Reference rs41543415(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324520C>A; NC_000006.11:g.31324520C>G; NC_000006.11:g.31324520C>T
CLNSRC
CLNACC