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rs398123305

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398123305(-;-)
Make rs398123305(-;AG)
Make rs398123305(AG;AG)
ReferenceGRCh38 38.1/141
Chromosome6
Position42978460
GenePEX6
is asnp
is mentioned by
dbSNPrs398123305
ebirs398123305
HLIrs398123305
Exacrs398123305
Varsomers398123305
Maprs398123305
PheGenIrs398123305
hapmaprs398123305
1000 genomesrs398123305
hgdprs398123305
ensemblrs398123305
gopubmedrs398123305
geneviewrs398123305
scholarrs398123305
googlers398123305
pharmgkbrs398123305
gwascentralrs398123305
openSNPrs398123305
23andMers398123305
23andMe allrs398123305
SNP Nexus

SNPshotrs398123305
SNPdbers398123305
MSV3drs398123305
GWAS Ctlgrs398123305
Max Magnitude0
ClinVar
Risk rs398123305(AG;AG)
Alt rs398123305(AG;AG)
Reference rs398123305(;)
Significance Pathogenic
Disease not provided Peroxisome biogenesis disorder 4a (zellweger)
Variation info
Gene PEX6
CLNDBN not provided Peroxisome biogenesis disorder 4a (zellweger)
Reversed 1
HGVS NC_000006.11:g.42946199_42946200dupCT
CLNSRC HGMD
CLNACC RCV000078577.3, RCV000173099.1,