Variant "IFIH1:c.2767A>G(p.Ile923Val)"
Search results: 2 records
Variant information
Gene:
Variant:
IFIH1:c.2767A>G(p.Ile923Val)
Genomic location:
chr2:163124637(hg19)
HGVS:
SO Term | RefSeq |
---|---|
protein_coding | NM_022168.3:c.2767A>G(p.Ile923Val) |
Alias:
IFIH1:I923V
dbSNP ID:
GWAS trait:
Modifier statisitcs
Record:
2
Disorder:
1
Reference:
1
Effect type:
Expressivity(2)
Modifier effect:
Risk factor(2)
Details: