Variant (rsID / SNP)

rs397516139

rs397516139 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYH7. Location: chromosome 14, position 23,894,961. Clinical significance in the table: Likely benign.

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Reference-table entries

MYH7Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 14:23894961
Cytoband: 14q11.2
HGVS: NM_000257.4(MYH7):c.2229G>A (p.Glu743=)
Allele change: Missense_E743D

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.