Variant "IL23R:c.1084G>A(p.Val362Ile)"
Search results: 3 records
Variant information
Gene:
Variant:
IL23R:c.1084G>A(p.Val362Ile)
Genomic location:
chr1:67705900(hg19)
HGVS:
SO Term | RefSeq |
---|---|
protein_coding | NM_144701.2:c.1084G>A(p.Val362Ile) |
Alias:
IL23R:V362I, IL23R:p.Val362Ile
dbSNP ID:
GWAS trait:
no data
Modifier statisitcs
Record:
3
Disorder:
2
Reference:
2
Effect type:
Expressivity(2)
,Penetrance(1)
Modifier effect:
Risk factor(2)
,Altered incidence(1)
Details: