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rs397514502

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397514502(C;G)
Make rs397514502(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position42693321
GeneA4GALT
is asnp
is mentioned by
dbSNPrs397514502
ebirs397514502
HLIrs397514502
Exacrs397514502
Varsomers397514502
Maprs397514502
PheGenIrs397514502
hapmaprs397514502
1000 genomesrs397514502
hgdprs397514502
ensemblrs397514502
gopubmedrs397514502
geneviewrs397514502
scholarrs397514502
googlers397514502
pharmgkbrs397514502
gwascentralrs397514502
openSNPrs397514502
23andMers397514502
23andMe allrs397514502
SNP Nexus

SNPshotrs397514502
SNPdbers397514502
MSV3drs397514502
GWAS Ctlgrs397514502
Max Magnitude0
ClinVar
Risk rs397514502(G;G)
Alt rs397514502(G;G)
Reference rs397514502(C;C)
Significance Other
Disease p phenotype
Variation info
Gene A4GALT
CLNDBN p phenotype
Reversed 1
HGVS NC_000022.10:g.43089327G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000032632.3,