Variant "ZFHX4:c.4916C>T(p.Ala1639Val)"
Search result: 1 record
Variant information
Gene:
Variant:
ZFHX4:c.4916C>T(p.Ala1639Val)
Genomic location:
chr8:77764073(hg19)
HGVS:
SO Term | RefSeq |
---|---|
protein_coding | NM_024721.4:c.4916C>T(p.Ala1639Val) |
dbSNP ID:
GWAS trait:
no data
Modifier statisitcs
Record:
1
Disorder:
1
Reference:
1
Effect type:
Expressivity(1)
Modifier effect:
Altered white blood cell counts(1)
Detail: