Variant (rsID / SNP)
rs3743057
rs3743057 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADAMTS7. Location: chromosome 15, position 79,089,007. Clinical significance in the table: Benign.
Reference-table entries
ADAMTS7Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- synonymous_variant
- Chromosome / position
- 15:79089007
- HGVS
- NM_014272.5,c.744A>G,p.Val248Val
- Allele change
- Synonymous_V248V
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.