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rs41559314

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41559314(A;A)
Make rs41559314(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356690
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41559314
ebirs41559314
HLIrs41559314
Exacrs41559314
Varsomers41559314
Maprs41559314
PheGenIrs41559314
hapmaprs41559314
1000 genomesrs41559314
hgdprs41559314
ensemblrs41559314
gopubmedrs41559314
geneviewrs41559314
scholarrs41559314
googlers41559314
pharmgkbrs41559314
gwascentralrs41559314
openSNPrs41559314
23andMers41559314
23andMe allrs41559314
SNP Nexus

SNPshotrs41559314
SNPdbers41559314
MSV3drs41559314
GWAS Ctlgrs41559314
Max Magnitude0
ClinVar
Risk rs41559314(A,G;A,G)
Alt rs41559314(A,G;A,G)
Reference rs41559314(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324467G>C; NC_000006.11:g.31324467G>T
CLNSRC
CLNACC