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Variant (rsID / SNP)

rs17535963

TRPM3

rs17535963 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRPM3. Location: chromosome 9, position 73,150,873. The table records no clinical significance for this variant.

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Reference-table entries

TRPM3Not classified
Variant type
missense_variant
Chromosome / position
9:73150873
HGVS
NM_001366147.2,c.5231A>C,p.Asn1744Thr
Allele change
Missense_N1554T

Associated conditions / phenotypes

Missense_N1579T|Missense_N1544T

Public references

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