Variant (rsID / SNP)

rs730880665

rs730880665 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYBPC3. Location: chromosome 11, position 47,355,268. The table records no clinical significance for this variant.

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Reference-table entries

MYBPC3Not classified

Variant type: Microsatellite
Chromosome / position: 11:47355268
Cytoband: 11p11.2
HGVS: NM_000256.3(MYBPC3):c.3029_3030del (p.Glu1010fs)

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.