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Variant (rsID / SNP)

rs1998233

TRPC4AP

rs1998233 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRPC4AP. Location: chromosome 20, position 33,657,126. The table records no clinical significance for this variant.

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Reference-table entries

TRPC4APNot classified
Variant type
synonymous_variant
Chromosome / position
20:33657126
HGVS
NM_015638.3,c.387C>T,p.Tyr129Tyr
Allele change
Synonymous_Y129Y

Public references

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