Variant "NRF1:c.1349-2857C>G"
Search result: 1 record
Variant information
Gene:
Variant:
NRF1:c.1349-2857C>G
Genomic location:
chr7:129381156(hg19)
HGVS:
SO Term | RefSeq |
---|---|
protein_coding | NM_001293163.1:c.1349-2857C>G |
protein_coding | NM_001293164.1:c.866-13702C>G |
protein_coding | NM_005011.4:c.1349-13702C>G |
protein_coding | NM_001040110.1:c.1349-13702C>G |
dbSNP ID:
GWAS trait:
no data
Modifier statisitcs
Record:
1
Disorder:
1
Reference:
1
Effect type:
Expressivity(1)
Modifier effect:
Risk factor(1)
Detail: