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rs398123812

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123812(C;T)
Make rs398123812(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position94603406
GeneSGCE
is asnp
is mentioned by
dbSNPrs398123812
ebirs398123812
HLIrs398123812
Exacrs398123812
Varsomers398123812
Maprs398123812
PheGenIrs398123812
hapmaprs398123812
1000 genomesrs398123812
hgdprs398123812
ensemblrs398123812
gopubmedrs398123812
geneviewrs398123812
scholarrs398123812
googlers398123812
pharmgkbrs398123812
gwascentralrs398123812
openSNPrs398123812
23andMers398123812
23andMe allrs398123812
SNP Nexus

SNPshotrs398123812
SNPdbers398123812
MSV3drs398123812
GWAS Ctlgrs398123812
Max Magnitude0
ClinVar
Risk rs398123812(T;T)
Alt rs398123812(T;T)
Reference rs398123812(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SGCE
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.94232718G>A
CLNSRC HGMD
CLNACC RCV000080356.4,