Variant "LTA4H:c.1059+160T>C"
Search results: 2 records
Variant information
Gene:
Variant:
LTA4H:c.1059+160T>C
Genomic location:
chr12:96409201(hg19)
HGVS:
SO Term | RefSeq |
---|---|
protein_coding | NM_000895.2:c.1059+160T>C |
pseudogene | NR_132659.1:n.1140+160T>C |
protein_coding | NM_001256643.1:c.987+160T>C |
protein_coding | NM_001256644.1:c.987+160T>C |
dbSNP ID:
GWAS trait:
no data
Modifier statisitcs
Record:
2
Disorder:
2
Reference:
1
Effect type:
Expressivity(2)
Modifier effect:
Risk factor(2)
Details: