Variant (rsID / SNP)

rs567723663

rs567723663 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYL3. Location: chromosome 3, position 46,899,961. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

MYL3Likely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 3:46899961
Cytoband: 3p21.31
HGVS: NM_000258.3(MYL3):c.482-10C>T
Allele change: Silent

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.