Variant (rsID / SNP)

rs6089088

rs6089088 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYLK2. Location: chromosome 20, position 30,414,621. Clinical significance in the table: Benign.

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Reference-table entries

MYLK2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 20:30414621
Cytoband: 20q11.21
HGVS: NM_033118.4(MYLK2):c.1104C>T (p.Phe368=)
Allele change: Synonymous_F368F

Associated conditions / phenotypes

Hypertrophic cardiomyopathy 1

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.