Variant (rsID / SNP)

rs201626

rs201626 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYH3. Location: chromosome 17, position 10,541,741. Clinical significance in the table: Benign.

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Reference-table entries

MYH3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:10541741
Cytoband: 17p13.1
HGVS: NM_002470.4(MYH3):c.3348T>C (p.Ile1116=)
Allele change: Synonymous_I1116I

Associated conditions / phenotypes

Freeman-Sheldon syndrome|Distal arthrogryposis type 2B1

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.