Variant "Intergenic:n.7106289T>C"
Search result: 1 record
Variant information
Gene:
Variant:
Intergenic:n.7106289T>C
Genomic location:
chr20:7106289(hg19)
HGVS:
SO Term | RefSeq |
---|---|
BMP2-LINC01428:n.7106289T>C |
dbSNP ID:
GWAS trait:
Modifier statisitcs
Record:
1
Disorder:
1
Reference:
1
Effect type:
Penetrance(1)
Modifier effect:
Altered incidence(1)
Detail: