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rs75402393

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs75402393(-;-)
Make rs75402393(-;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356974
GeneHLA-B
is asnp
is mentioned by
dbSNPrs75402393
ebirs75402393
HLIrs75402393
Exacrs75402393
Varsomers75402393
Maprs75402393
PheGenIrs75402393
hapmaprs75402393
1000 genomesrs75402393
hgdprs75402393
ensemblrs75402393
gopubmedrs75402393
geneviewrs75402393
scholarrs75402393
googlers75402393
pharmgkbrs75402393
gwascentralrs75402393
openSNPrs75402393
23andMers75402393
23andMe allrs75402393
SNP Nexus

SNPshotrs75402393
SNPdbers75402393
MSV3drs75402393
GWAS Ctlgrs75402393
Max Magnitude0
ClinVar
Risk rs75402393(;)
Alt rs75402393(;)
Reference rs75402393(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324751delG
CLNSRC
CLNACC