rs28939678
From SNPedia
Merged into | rs121434455 |
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 |
Make rs28939678(C;C) |
Make rs28939678(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 92504812 |
Gene | PEX1 |
is a | snp |
is | mentioned by |
dbSNP | rs28939678 |
dbSNP (classic) | rs28939678 |
ClinGen | rs28939678 |
ebi | rs28939678 |
HLI | rs28939678 |
Exac | rs28939678 |
Gnomad | rs28939678 |
Varsome | rs28939678 |
LitVar | rs28939678 |
Map | rs28939678 |
PheGenI | rs28939678 |
Biobank | rs28939678 |
1000 genomes | rs28939678 |
hgdp | rs28939678 |
ensembl | rs28939678 |
geneview | rs28939678 |
scholar | rs28939678 |
rs28939678 | |
pharmgkb | rs28939678 |
gwascentral | rs28939678 |
openSNP | rs28939678 |
23andMe | rs28939678 |
SNPshot | rs28939678 |
SNPdbe | rs28939678 |
MSV3d | rs28939678 |
GWAS Ctlg | rs28939678 |
Status | Merged into rs121434455 |
Max Magnitude | 0 |
[PMID 11439091] Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction.