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rs387906280

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs387906280(-;-)
Make rs387906280(-;C)
Make rs387906280(C;C)
ReferenceGRCh38 38.1/141
Chromosome22
Position42692922
GeneA4GALT
is asnp
is mentioned by
dbSNPrs387906280
ebirs387906280
HLIrs387906280
Exacrs387906280
Varsomers387906280
Maprs387906280
PheGenIrs387906280
hapmaprs387906280
1000 genomesrs387906280
hgdprs387906280
ensemblrs387906280
gopubmedrs387906280
geneviewrs387906280
scholarrs387906280
googlers387906280
pharmgkbrs387906280
gwascentralrs387906280
openSNPrs387906280
23andMers387906280
23andMe allrs387906280
SNP Nexus

SNPshotrs387906280
SNPdbers387906280
MSV3drs387906280
GWAS Ctlgrs387906280
Max Magnitude0
ClinVar
Risk rs387906280(C;C)
Alt rs387906280(C;C)
Reference rs387906280(;)
Significance Other
Disease p phenotype
Variation info
Gene A4GALT
CLNDBN p phenotype
Reversed 1
HGVS NC_000022.10:g.43088929dupG
CLNSRC OMIM Allelic Variant
CLNACC RCV000002816.3,