Variant "SLC38A8:c.1163-58T>C"
Search result: 1 record
Variant information
Gene:
Variant:
SLC38A8:c.1163-58T>C
Genomic location:
chr16:84046715(hg19)
HGVS:
SO Term | RefSeq |
---|---|
protein_coding | NM_001080442.2:c.1163-58T>C |
dbSNP ID:
GWAS trait:
Modifier statisitcs
Record:
1
Disorder:
1
Reference:
1
Effect type:
Expressivity(1)
Modifier effect:
Altered severity(1)
Detail: