Variant (rsID / SNP)

rs17707947

rs17707947 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYO10. Location: chromosome 5, position 16,877,744. The table records no clinical significance for this variant.

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Reference-table entries

MYO10Not classified

Variant type: missense_variant
Chromosome / position: 5:16877744
HGVS: NM_012334.3,c.94G>A,p.Val32Ile
Allele change: Missense_V32I

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.