Variant (rsID / SNP)

rs61735441

rs61735441 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KIAA0753. Location: chromosome 17, position 6,511,741. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

KIAA0753Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 17:6511741
Cytoband: 17p13.1
HGVS: NM_014804.3(KIAA0753):c.1756A>G (p.Lys586Glu)
Allele change: Silent

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.