Variant (rsID / SNP)

rs367742240

rs367742240 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYH6. Location: chromosome 14, position 23,866,770. Clinical significance in the table: Likely benign.

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Reference-table entries

MYH6Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 14:23866770
Cytoband: 14q11.2
HGVS: NM_002471.4(MYH6):c.1944G>A (p.Thr648=)
Allele change: Synonymous_T648T

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.