Variant "HMGCR:c.1722+45A>G"
Search results: 2 records
Variant information
Gene:
Variant:
HMGCR:c.1722+45A>G
Genomic location:
chr5:74651084(hg19)
HGVS:
SO Term | RefSeq |
---|---|
protein_coding | NM_000859.2:c.1722+45A>G |
protein_coding | NM_001130996.1:c.1564-106A>G |
dbSNP ID:
GWAS trait:
Modifier statisitcs
Record:
2
Disorder:
1
Reference:
2
Effect type:
Expressivity(1)
,Penetrance(1)
Modifier effect:
Altered incidence(1)
,Altered severity and onset time(1)
Details: