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Variant (rsID / SNP)

rs674155

RYR3

rs674155 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RYR3. Location: chromosome 15, position 33,872,177. The table records no clinical significance for this variant.

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Reference-table entries

RYR3Not classified
Variant type
splice_region_variant&synonymous_variant
Chromosome / position
15:33872177
HGVS
NM_001036.6,c.1269C>T,p.Ser423Ser
Allele change
Synonymous_S423S

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.