Variant "PROX1:n.506-18260C>A"
Search result: 1 record
Variant information
Gene:
Variant:
PROX1:n.506-18260C>A
Genomic location:
chr1:214024225(hg19)
HGVS:
SO Term | RefSeq |
---|---|
pseudogene | NR_037850.2:n.506-18260C>A |
dbSNP ID:
GWAS trait:
Modifier statisitcs
Record:
1
Disorder:
1
Reference:
1
Effect type:
Expressivity(1)
Modifier effect:
Risk factor(1)
Detail: