Variant (rsID / SNP)

rs61753652

rs61753652 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYO1C. Location: chromosome 17, position 1,372,861. Clinical significance in the table: Benign.

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Reference-table entries

MYO1CBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:1372861
Cytoband: 17p13.3
HGVS: NM_001080779.2(MYO1C):c.2574A>C (p.Lys858Asn)
Allele change: Missense_K858N

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.