Variant "NOS1AP:n.162033890C>T"
Search results: 4 records
Variant information
Gene:
Variant:
NOS1AP:n.162033890C>T
Genomic location:
chr1:162033890(hg19)
HGVS:
SO Term | RefSeq |
---|---|
OLFML2B-NOS1AP:n.162033890C>T |
Alias:
NOS1AP:rs12143842
dbSNP ID:
GWAS trait:
Modifier statisitcs
Record:
4
Disorder:
1
Reference:
4
Effect type:
Expressivity(4)
Modifier effect:
Altered severity(2)
,Risk factor(2)
Details: