Variant "BMPR2:c.1413+3181G>C"
Search results: 2 records
Variant information
Gene:
Variant:
BMPR2:c.1413+3181G>C
Genomic location:
chr2:203410351(hg19)
HGVS:
SO Term | RefSeq |
---|---|
protein_coding | NM_001204.6:c.1413+3181G>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: