Variant "NCAN:c.274C>T(p.Pro92Ser)"
Search result: 1 record
Variant information
Gene:
Variant:
NCAN:c.274C>T(p.Pro92Ser)
Genomic location:
chr19:19329924(hg19)
HGVS:
SO Term | RefSeq |
---|---|
protein_coding | NM_004386.2:c.274C>T(p.Pro92Ser) |
dbSNP ID:
GWAS trait:
Modifier statisitcs
Record:
1
Disorder:
1
Reference:
1
Effect type:
Expressivity(1)
Modifier effect:
Altered severity(1)
Detail: