Variant (rsID / SNP)

rs10615

rs10615 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DEAF1. Location: chromosome 11, position 653,968. Clinical significance in the table: Benign.

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Reference-table entries

DEAF1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 11:653968
Cytoband: 11p15.5
HGVS: NM_021008.4(DEAF1):c.1587A>G (p.Gln529=)
Allele change: Synonymous_Q529Q

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.