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rs41545614

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41545614(G;T)
Make rs41545614(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356420
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41545614
ebirs41545614
HLIrs41545614
Exacrs41545614
Varsomers41545614
Maprs41545614
PheGenIrs41545614
hapmaprs41545614
1000 genomesrs41545614
hgdprs41545614
ensemblrs41545614
gopubmedrs41545614
geneviewrs41545614
scholarrs41545614
googlers41545614
pharmgkbrs41545614
gwascentralrs41545614
openSNPrs41545614
23andMers41545614
23andMe allrs41545614
SNP Nexus

SNPshotrs41545614
SNPdbers41545614
MSV3drs41545614
GWAS Ctlgrs41545614
Max Magnitude0
ClinVar
Risk rs41545614(A,T;A,T)
Alt rs41545614(A,T;A,T)
Reference rs41545614(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324197C>A; NC_000006.11:g.31324197C>T
CLNSRC
CLNACC