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Variant (rsID / SNP)

rs1274958

CSRNP1

rs1274958 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CSRNP1. Location: chromosome 3, position 39,184,959. The table records no clinical significance for this variant.

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Reference-table entries

CSRNP1Not classified
Variant type
missense_variant
Chromosome / position
3:39184959
HGVS
NM_001320559.2,c.1417G>A,p.Val473Ile
Allele change
Missense_V453I

Public references

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