Have questions? Visit https://www.reddit.com/r/SNPedia

rs398123301

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs398123301(-;-)
Make rs398123301(-;CT)
ReferenceGRCh38 38.1/141
Chromosome17
Position35575973
GenePEX12
is asnp
is mentioned by
dbSNPrs398123301
ebirs398123301
HLIrs398123301
Exacrs398123301
Varsomers398123301
Maprs398123301
PheGenIrs398123301
hapmaprs398123301
1000 genomesrs398123301
hgdprs398123301
ensemblrs398123301
gopubmedrs398123301
geneviewrs398123301
scholarrs398123301
googlers398123301
pharmgkbrs398123301
gwascentralrs398123301
openSNPrs398123301
23andMers398123301
23andMe allrs398123301
SNP Nexus

SNPshotrs398123301
SNPdbers398123301
MSV3drs398123301
GWAS Ctlgrs398123301
Max Magnitude0
ClinVar
Risk rs398123301(;)
Alt rs398123301(;)
Reference rs398123301(CT;CT)
Significance Pathogenic
Disease not provided
Variation info
Gene PEX12
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.33902992_33902993delAG
CLNSRC HGMD
CLNACC RCV000078563.4,