Variant (rsID / SNP)

rs6678540

rs6678540 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYOM3. Location: chromosome 1, position 24,421,474. The table records no clinical significance for this variant.

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Reference-table entries

MYOM3Not classified

Variant type: missense_variant
Chromosome / position: 1:24421474
HGVS: NM_152372.4,c.797C>T,p.Thr266Met
Allele change: Missense_T266M

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.