Variant "STS:c.1399+2333C>G"
Search result: 1 record
Variant information
Gene:
Variant:
STS:c.1399+2333C>G
Genomic location:
chrX:7254481(hg19)
HGVS:
SO Term | RefSeq |
---|---|
protein_coding | NM_001320750.1:c.1399+2333C>G |
protein_coding | NM_001320751.1:c.1399+2333C>G |
protein_coding | NM_001320752.1:c.1399+2333C>G |
protein_coding | NM_000351.5:c.1378+2333C>G |
protein_coding | NM_001320753.1:c.1363+2333C>G |
show all |
dbSNP ID:
GWAS trait:
no data
Modifier statisitcs
Record:
1
Disorder:
1
Reference:
1
Effect type:
Expressivity(1)
Modifier effect:
Risk factor(1)
Detail: