Variant "NOS3:c.894T>G(p.Asp298Glu)"
Search results: 6 records
Variant information
Gene:
Variant:
NOS3:c.894T>G(p.Asp298Glu)
Genomic location:
chr7:150696111(hg19)
HGVS:
SO Term | RefSeq |
---|---|
protein_coding | NM_000603.4:c.894T>G(p.Asp298Glu) |
protein_coding | NM_001160109.1:c.894T>G(p.Asp298Glu) |
protein_coding | NM_001160110.1:c.894T>G(p.Asp298Glu) |
protein_coding | NM_001160111.1:c.894T>G(p.Asp298Glu) |
Alias:
NOS3:894G>T, NOS3:rs1799983
dbSNP ID:
GWAS trait:
no data
Modifier statisitcs
Record:
6
Disorder:
5
Reference:
5
Effect type:
Expressivity(5)
,Pleiotropy(1)
Modifier effect:
Risk factor(2)
,Altered airway nitric oxide formation(1)
,Altered annual rate of FEV1(1)
,Altered onset time(1)
,Altered severity(1)
Details: