Variant "MBNL1:n.*1846T>C"
Search result: 1 record
Variant information
Gene:
Variant:
MBNL1:n.*1846T>C
Genomic location:
chr3:151978559(hg19)
HGVS:
SO Term | RefSeq |
---|---|
pseudogene | NR_027038.1:n.*1846T>C |
pseudogene | NR_027037.1:n.*1846T>C |
LOC101928166-MBNL1-AS1:n.151978559A>G |
dbSNP ID:
GWAS trait:
no data
Modifier statisitcs
Record:
1
Disorder:
1
Reference:
1
Effect type:
Expressivity(1)
Modifier effect:
Altered severity(1)
Detail: