Variant "SLC22A7:c.*1364T>C"
Search result: 1 record
Variant information
Gene:
Variant:
SLC22A7:c.*1364T>C
Genomic location:
chr6:43272188(hg19)
HGVS:
SO Term | RefSeq |
---|---|
protein_coding | NM_206922.2:c.*1364T>C |
protein_coding | NM_153320.2:c.1592+206A>G |
protein_coding | NM_006672.3:c.1586+206A>G |
dbSNP ID:
GWAS trait:
Modifier statisitcs
Record:
1
Disorder:
1
Reference:
1
Effect type:
Expressivity(1)
Modifier effect:
Risk factor(1)
Detail: