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Variant (rsID / SNP)

rs9868484

MYH15

rs9868484 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYH15. Location: chromosome 3, position 108,188,993. The table records no clinical significance for this variant.

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Reference-table entries

MYH15Not classified
Variant type
missense_variant
Chromosome / position
3:108188993
HGVS
NM_014981.3,c.1450C>T,p.His484Tyr
Allele change
Missense_H504Y

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.