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rs1028247729

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position92522246
GenePEX1
is asnp
is mentioned by
dbSNPrs1028247729
dbSNP (old)rs1028247729
ClinGenrs1028247729
ebirs1028247729
HLIrs1028247729
Exacrs1028247729
Gnomadrs1028247729
Varsomers1028247729
LitVarrs1028247729
Maprs1028247729
PheGenIrs1028247729
Biobankrs1028247729
1000 genomesrs1028247729
hgdprs1028247729
ensemblrs1028247729
gopubmedrs1028247729
geneviewrs1028247729
scholarrs1028247729
googlers1028247729
pharmgkbrs1028247729
gwascentralrs1028247729
openSNPrs1028247729
23andMers1028247729
23andMe allrs1028247729
SNPshotrs1028247729
SNPdbers1028247729
MSV3drs1028247729
GWAS Ctlgrs1028247729
Max Magnitude0
ClinVar
Risk rs1028247729(A;A)
Alt rs1028247729(A;A)
Reference Rs1028247729(C;C)
Significance Probable-Pathogenic
Disease Zellweger syndrome Peroxisome biogenesis disorder 1B
Variation info
Gene
CLNDBN Zellweger syndrome Peroxisome biogenesis disorder 1B
Reversed 0
HGVS NC_000007.13:g.92151560C>G
CLNSRC
CLNACC RCV000411284.1, RCV000412347.1,