Variant (rsID / SNP)

rs117696188

rs117696188 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYO1C. Location: chromosome 17, position 1,383,868. Clinical significance in the table: Likely benign.

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Reference-table entries

MYO1CLikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 17:1383868
Cytoband: 17p13.3
HGVS: NM_001080779.2(MYO1C):c.859G>A (p.Val287Ile)
Allele change: Missense_V287I

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.