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rs41548617

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41548617(C;C)
Make rs41548617(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356220
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41548617
ebirs41548617
HLIrs41548617
Exacrs41548617
Varsomers41548617
Maprs41548617
PheGenIrs41548617
hapmaprs41548617
1000 genomesrs41548617
hgdprs41548617
ensemblrs41548617
gopubmedrs41548617
geneviewrs41548617
scholarrs41548617
googlers41548617
pharmgkbrs41548617
gwascentralrs41548617
openSNPrs41548617
23andMers41548617
23andMe allrs41548617
SNP Nexus

SNPshotrs41548617
SNPdbers41548617
MSV3drs41548617
GWAS Ctlgrs41548617
Max Magnitude0
ClinVar
Risk rs41548617(C,G;C,G)
Alt rs41548617(C,G;C,G)
Reference rs41548617(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323997A>C; NC_000006.11:g.31323997A>G
CLNSRC
CLNACC