Variant (rsID / SNP)

rs199900004

rs199900004 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYOM1. Location: chromosome 18, position 3,129,368. Clinical significance in the table: Likely benign.

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Reference-table entries

MYOM1Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 18:3129368
Cytoband: 18p11.31
HGVS: NM_003803.4(MYOM1):c.2656A>G (p.Ser886Gly)
Allele change: Missense_S886G

Associated conditions / phenotypes

Hypertrophic cardiomyopathy

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.