LOVD - Variant listings for ADAMTS2

About this overview [Show]

Patient data (#0001839)
Patient ID
Disease -
Reference Arning et al., 2012
Template DNA
Technique WGS
Remarks This SNP is highly associated with pediatric stroke.
Ethnic origin -

Variant data
Allele Unknown
Reported pathogenicity No known pathogenicity
Concluded pathogenicity No known pathogenicity
Exon 3i
DNA change c.689-28692T>G   (View in UCSC Genome Browser, Ensembl)
dbSNP dbSNP
Type Substitution
Mutation Effect Other
Protein -
RNA change -
Re-site -
Frequency -
DB-ID ADAMTS2_00016

1 entry in ADAMTS2

Path.
Allele Descending
Ascending
Exon Descending
Ascending
DNA change Descending
Ascending
dbSNP Descending
Ascending
Type Descending
Ascending
Mutation Effect Descending
Ascending
Protein Descending
Ascending
RNA change Descending
Ascending
Re-site Descending
Ascending
Frequency Descending
Ascending
DB-ID Descending
Ascending
-/- Unknown 3i c.689-28692T>G dbSNP Substitution Other - - - - ADAMTS2_00016