Variant (rsID / SNP)

rs182236729

rs182236729 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYH7B. Location: chromosome 20, position 33,581,971. Clinical significance in the table: Uncertain significance.

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Reference-table entries

MYH7BUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 20:33581971
Cytoband: 20q11.22
HGVS: NM_020884.7(MYH7B):c.2467T>C (p.Trp823Arg)
Allele change: Missense_W865R

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.