Variant (rsID / SNP)

rs148240352

rs148240352 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MAGI2. Location: chromosome 7, position 79,082,418. Clinical significance in the table: Conflicting interpretations of pathogenicity.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

MAGI2Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 7:79082418
Cytoband: 7q21.11
HGVS: NM_012301.4(MAGI2):c.219C>T (p.Pro73=)
Allele change: Synonymous_P73P

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.