Variant "ALPL:c.1190-65C>A"
Search result: 1 record
Variant information
Gene:
Variant:
ALPL:c.1190-65C>A 
Genomic location:
chr1:21902950(hg19) 
HGVS:
SO Term RefSeq
protein_coding NM_000478.5:c.1190-65C>A
protein_coding NM_001127501.3:c.1025-65C>A
protein_coding NM_001177520.2:c.959-65C>A
dbSNP ID:
GWAS trait:
no data 
Modifier statisitcs
Record:
Disorder:
Reference:
Effect type:
Expressivity(1)  
Modifier effect:
Risk factor(1)  
Detail:
  • Target disease:
    Effect type:
    Expressivity 
    Modifier effect:
    Risk factor 
    Evidence:
    P=0.01 
    Effect:
    The SNV c.1190-65C>A (rs1780329) in the ALP gene was significantly more frequent in PXE patients.
    Reference:
    Title:
    Variants in genes encoding pyrophosphate metabolizing enzymes are associated with Pseudoxanthoma elasticum.
    Species studied:
    Human
    Abstract:
    Pseudoxanthoma elasticum (PXE) is a rare hereditary disorder characterized by progressive calcification and fragmentation of elastic fibers. Because of the great clinical variability between PXE patients the involvement of modifier genes was recently suggested. Therefore, we investigated the association of single nucleotide variants (SNVs) in selected candidate genes known to regulate cellular pyrophosphate metabolism.