Variant (rsID / SNP)
rs2074641
rs2074641 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MAGI2. Location: chromosome 7, position 77,756,580. Clinical significance in the table: Benign.
Reference-table entries
MAGI2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 7:77756580
- Cytoband
- 7q21.11
- HGVS
- NM_012301.4(MAGI2):c.3357A>G (p.Leu1119=)
- Allele change
- Synonymous_L1105L
Associated conditions / phenotypes
Nephrotic syndrome 15
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.