Variant (rsID / SNP)

rs57132842

rs57132842 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RYR1. Location: chromosome 19, position 38,935,366. Clinical significance in the table: Benign.

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Reference-table entries

RYR1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 19:38935366
Cytoband: 19q13.2
HGVS: NM_000540.3(RYR1):c.631+49C>T
Allele change: Silent

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.