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Variant (rsID / SNP)

rs800342

TRPM5

rs800342 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRPM5. Location: chromosome 11, position 2,427,291. The table records no clinical significance for this variant.

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Reference-table entries

TRPM5Not classified
Variant type
synonymous_variant
Chromosome / position
11:2427291
HGVS
NM_014555.4,c.3282T>G,p.Gly1094Gly
Allele change
Synonymous_G1094G

Public references

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