Variant (rsID / SNP)

rs34937835

rs34937835 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MAGI2. Location: chromosome 7, position 77,885,552. Clinical significance in the table: Benign.

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Reference-table entries

MAGI2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 7:77885552
Cytoband: 7q21.11
HGVS: NM_012301.4(MAGI2):c.1755C>T (p.Pro585=)
Allele change: Synonymous_P585P

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.