Variant (rsID / SNP)

rs121913653

rs121913653 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYH7. Location: chromosome 14, position 23,898,249. Clinical significance in the table: Benign.

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Reference-table entries

MYH7Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 14:23898249
Cytoband: 14q11.2
HGVS: NM_000257.4(MYH7):c.1322C>T (p.Thr441Met)
Allele change: Missense_T441M

Associated conditions / phenotypes

MYH7-related skeletal myopathy|Cardiomyopathy|Hypertrophic cardiomyopathy 1|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.