Variant "SAMM50:c.21+2633C>T"
Search result: 1 record
Variant information
Gene:
Variant:
SAMM50:c.21+2633C>T
Genomic location:
chr22:44354111(hg19)
HGVS:
SO Term | RefSeq |
---|---|
protein_coding | NM_015380.4:c.21+2633C>T |
dbSNP ID:
GWAS trait:
Modifier statisitcs
Record:
1
Disorder:
1
Reference:
1
Effect type:
Expressivity(1)
Modifier effect:
Altered severity(1)
Detail: