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rs41559614

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41559614(A;A)
Make rs41559614(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355348
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41559614
ebirs41559614
HLIrs41559614
Exacrs41559614
Varsomers41559614
Maprs41559614
PheGenIrs41559614
hapmaprs41559614
1000 genomesrs41559614
hgdprs41559614
ensemblrs41559614
gopubmedrs41559614
geneviewrs41559614
scholarrs41559614
googlers41559614
pharmgkbrs41559614
gwascentralrs41559614
openSNPrs41559614
23andMers41559614
23andMe allrs41559614
SNP Nexus

SNPshotrs41559614
SNPdbers41559614
MSV3drs41559614
GWAS Ctlgrs41559614
Max Magnitude0
ClinVar
Risk rs41559614(A;A)
Alt rs41559614(A;A)
Reference rs41559614(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323125C>T
CLNSRC
CLNACC