Variant "ABCB4:c.711A>T(p.Ile237Ile)"
Search result: 1 record
Variant information
Gene:
Variant:
ABCB4:c.711A>T(p.Ile237Ile)
Genomic location:
chr7:87079406(hg19)
HGVS:
SO Term | RefSeq |
---|---|
protein_coding | NM_018849.2:c.711A>T(p.Ile237Ile) |
protein_coding | NM_000443.3:c.711A>T(p.Ile237Ile) |
protein_coding | NM_018850.2:c.711A>T(p.Ile237Ile) |
dbSNP ID:
GWAS trait:
Modifier statisitcs
Record:
1
Disorder:
1
Reference:
1
Effect type:
Penetrance(1)
Modifier effect:
Altered incidence(1)
Detail: