Variant "SELP:c.1147+440G>A"
Search results: 2 records
Variant information
Gene:
Variant:
SELP:c.1147+440G>A
Genomic location:
chr1:169580290(hg19)
HGVS:
SO Term | RefSeq |
---|---|
protein_coding | NM_003005.3:c.1147+440G>A |
dbSNP ID:
GWAS trait:
Modifier statisitcs
Record:
2
Disorder:
2
Reference:
1
Effect type:
Expressivity(2)
Modifier effect:
Risk factor(2)
Details: