Variant (rsID / SNP)

rs1064794753

rs1064794753 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RYR2. Location: chromosome 1, position 237,947,581. 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: 1:237947581
Cytoband: 1q43
HGVS: NM_001035.3(RYR2):c.12569T>G (p.Val4190Gly)
Allele change: Missense_V4190G

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.