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rs398123409

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123409(C;T)
Make rs398123409(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position92502076
GenePEX1
is asnp
is mentioned by
dbSNPrs398123409
ebirs398123409
HLIrs398123409
Exacrs398123409
Varsomers398123409
Maprs398123409
PheGenIrs398123409
hapmaprs398123409
1000 genomesrs398123409
hgdprs398123409
ensemblrs398123409
gopubmedrs398123409
geneviewrs398123409
scholarrs398123409
googlers398123409
pharmgkbrs398123409
gwascentralrs398123409
openSNPrs398123409
23andMers398123409
23andMe allrs398123409
SNP Nexus

SNPshotrs398123409
SNPdbers398123409
MSV3drs398123409
GWAS Ctlgrs398123409
Max Magnitude0
ClinVar
Risk rs398123409(T;T)
Alt rs398123409(T;T)
Reference rs398123409(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PEX1
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.92131390G>A
CLNSRC ClinVar Emory University
CLNACC RCV000078919.4,