Variant (rsID / SNP)

rs34953692

rs34953692 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYH8. Location: chromosome 17, position 10,302,965. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

MYH8Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 17:10302965
Cytoband: 17p13.1
HGVS: NM_002472.3(MYH8):c.3757C>T (p.Arg1253Cys)
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.