Variant (rsID / SNP)

rs150351713

rs150351713 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYH8. Location: chromosome 17, position 10,310,061. Clinical significance in the table: Likely benign.

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Reference-table entries

MYH8Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 17:10310061
Cytoband: 17p13.1
HGVS: NM_002472.3(MYH8):c.2117G>A (p.Arg706His)
Allele change: Silent

Associated conditions / phenotypes

Hecht syndrome

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.