Variant (rsID / SNP)

rs74967762

rs74967762 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYH2. Location: chromosome 17, position 10,453,015. Clinical significance in the table: Likely benign.

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Reference-table entries

MYH2Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 17:10453015
Cytoband: 17p13.1
HGVS: NM_017534.5(MYH2):c.-126A>G
Allele change: Silent

Associated conditions / phenotypes

Inclusion Body Myopathy, Dominant

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.