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Variant (rsID / SNP)

rs4780144

RYR3

rs4780144 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RYR3. Location: chromosome 15, position 33,954,652. The table records no clinical significance for this variant.

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Reference-table entries

RYR3Not classified
Variant type
missense_variant
Chromosome / position
15:33954652
HGVS
NM_001036.6,c.4921C>T,p.Arg1641Cys
Allele change
Missense_R1641C

Public references

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