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Variant (rsID / SNP)

rs6560142

TRPM3

rs6560142 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRPM3. Location: chromosome 9, position 73,150,984. The table records no clinical significance for this variant.

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Reference-table entries

TRPM3Not classified
Variant type
missense_variant
Chromosome / position
9:73150984
HGVS
NM_001366147.2,c.5120G>A,p.Arg1707Gln
Allele change
Missense_R1517Q

Associated conditions / phenotypes

Missense_R1542Q|Missense_R1507Q

Public references

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