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rs41552318

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41552318(A;A)
Make rs41552318(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356942
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41552318
ebirs41552318
HLIrs41552318
Exacrs41552318
Varsomers41552318
Maprs41552318
PheGenIrs41552318
hapmaprs41552318
1000 genomesrs41552318
hgdprs41552318
ensemblrs41552318
gopubmedrs41552318
geneviewrs41552318
scholarrs41552318
googlers41552318
pharmgkbrs41552318
gwascentralrs41552318
openSNPrs41552318
23andMers41552318
23andMe allrs41552318
SNP Nexus

SNPshotrs41552318
SNPdbers41552318
MSV3drs41552318
GWAS Ctlgrs41552318
Max Magnitude0
ClinVar
Risk rs41552318(A,C;A,C)
Alt rs41552318(A,C;A,C)
Reference rs41552318(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324719C>G; NC_000006.11:g.31324719C>T
CLNSRC
CLNACC