Variant "FGFR2:c.109+906T>C"
Search results: 3 records
Variant information
Gene:
Variant:
FGFR2:c.109+906T>C
Genomic location:
chr10:123352317(hg19)
HGVS:
SO Term | RefSeq |
---|---|
protein_coding | NM_022970.3:c.109+906T>C |
protein_coding | NM_001144914.1:c.109+906T>C |
protein_coding | NM_023029.2:c.109+906T>C |
protein_coding | NM_001144916.1:c.109+906T>C |
protein_coding | NM_001144915.1:c.109+906T>C |
show all |
dbSNP ID:
GWAS trait:
Modifier statisitcs
Record:
3
Disorder:
2
Reference:
2
Effect type:
Expressivity(3)
Modifier effect:
Risk factor(3)
Details: