Variant "LPA:c.4289+1G>A"
Search results: 2 records
Variant information
Gene:
Variant:
LPA:c.4289+1G>A
Genomic location:
chr6:161006077(hg19)
HGVS:
SO Term | RefSeq |
---|---|
protein_coding | NM_005577.2:c.4289+1G>A |
dbSNP ID:
GWAS trait:
Modifier statisitcs
Record:
2
Disorder:
1
Reference:
1
Effect type:
Expressivity(1)
,Penetrance(1)
Modifier effect:
Altered incidence(1)
,Risk factor(1)
Details: