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rs41556614

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41556614(C;C)
Make rs41556614(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356784
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41556614
ebirs41556614
HLIrs41556614
Exacrs41556614
Varsomers41556614
Maprs41556614
PheGenIrs41556614
hapmaprs41556614
1000 genomesrs41556614
hgdprs41556614
ensemblrs41556614
gopubmedrs41556614
geneviewrs41556614
scholarrs41556614
googlers41556614
pharmgkbrs41556614
gwascentralrs41556614
openSNPrs41556614
23andMers41556614
23andMe allrs41556614
SNP Nexus

SNPshotrs41556614
SNPdbers41556614
MSV3drs41556614
GWAS Ctlgrs41556614
Max Magnitude0
ClinVar
Risk rs41556614(C;C)
Alt rs41556614(C;C)
Reference rs41556614(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324561A>G
CLNSRC
CLNACC