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rs398123408

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398123408(-;-)
Make rs398123408(-;CAGTGTGGA)
Make rs398123408(CAGTGTGGA;CAGTGTGGA)
ReferenceGRCh38 38.1/141
Chromosome7
Position92504842
GenePEX1
is asnp
is mentioned by
dbSNPrs398123408
ebirs398123408
HLIrs398123408
Exacrs398123408
Varsomers398123408
Maprs398123408
PheGenIrs398123408
hapmaprs398123408
1000 genomesrs398123408
hgdprs398123408
ensemblrs398123408
gopubmedrs398123408
geneviewrs398123408
scholarrs398123408
googlers398123408
pharmgkbrs398123408
gwascentralrs398123408
openSNPrs398123408
23andMers398123408
23andMe allrs398123408
SNP Nexus

SNPshotrs398123408
SNPdbers398123408
MSV3drs398123408
GWAS Ctlgrs398123408
Max Magnitude0
ClinVar
Risk rs398123408(CAGTGTGGA;CAGTGTGGA)
Alt rs398123408(CAGTGTGGA;CAGTGTGGA)
Reference rs398123408(;)
Significance Pathogenic
Disease not provided
Variation info
Gene PEX1
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.92134157_92134165dupTCCACACTG
CLNSRC HGMD
CLNACC RCV000078917.3,