Variant "ABCC2:c.3563T>A(p.Val1188Glu)"
Search result: 1 record
Variant information
Gene:
Variant:
ABCC2:c.3563T>A(p.Val1188Glu)
Genomic location:
chr10:101595996(hg19)
HGVS:
SO Term | RefSeq |
---|---|
protein_coding | NM_000392.4:c.3563T>A(p.Val1188Glu) |
dbSNP ID:
GWAS trait:
no data
Modifier statisitcs
Record:
1
Disorder:
1
Reference:
1
Effect type:
Expressivity(1)
Modifier effect:
Risk factor(1)
Detail: