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rs28939678

From SNPedia

Merged intors121434455
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0
Make rs28939678(C;C)
Make rs28939678(C;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position92504812
GenePEX1
is asnp
is mentioned by
dbSNPrs28939678
dbSNP (old)rs28939678
ClinGenrs28939678
ebirs28939678
HLIrs28939678
Exacrs28939678
Varsomers28939678
Maprs28939678
PheGenIrs28939678
Biobankrs28939678
1000 genomesrs28939678
hgdprs28939678
ensemblrs28939678
gopubmedrs28939678
geneviewrs28939678
scholarrs28939678
googlers28939678
pharmgkbrs28939678
gwascentralrs28939678
openSNPrs28939678
23andMers28939678
23andMe allrs28939678
SNP Nexus

SNPshotrs28939678
SNPdbers28939678
MSV3drs28939678
GWAS Ctlgrs28939678
StatusMerged into rs121434455
Max Magnitude0
OMIM602136
DescZELLWEGER SYNDROME
Variant0002
Relatedalso
[PMID 11439091OA-icon.png] Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction.