Variant (rsID / SNP)

rs730880199

rs730880199 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RYR2. Location: chromosome 1, position 237,982,467. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

RYR2Likely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 1:237982467
Cytoband: 1q43
HGVS: NM_001035.3(RYR2):c.14565T>G (p.Ile4855Met)
Allele change: Missense_I4855M

Associated conditions / phenotypes

Left ventricular noncompaction cardiomyopathy

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.