Variant "LINC00951:n.1988T>C"
Search result: 1 record
Variant information
Gene:
Variant:
LINC00951:n.1988T>C
Genomic location:
chr6:40321758(hg19)
HGVS:
SO Term | RefSeq |
---|---|
pseudogene | NR_038887.1:n.1988T>C |
dbSNP ID:
GWAS trait:
no data
Modifier statisitcs
Record:
1
Disorder:
1
Reference:
1
Effect type:
Expressivity(1)
Modifier effect:
Risk factor(1)
Detail: