Variant "HNMT:c.191-12449C>A"
Search result: 1 record
Variant information
Gene:
Variant:
HNMT:c.191-12449C>A
Genomic location:
chr2:138746039(hg19)
HGVS:
SO Term | RefSeq |
---|---|
protein_coding | NM_006895.2:c.191-12449C>A |
dbSNP ID:
GWAS trait:
no data
Modifier statisitcs
Record:
1
Disorder:
1
Reference:
1
Effect type:
Expressivity(1)
Modifier effect:
Risk factor(1)
Detail: