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Variant (rsID / SNP)

rs17868387

TRPM8

rs17868387 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRPM8. Location: chromosome 2, position 234,854,552. The table records no clinical significance for this variant.

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Reference-table entries

TRPM8Not classified
Variant type
missense_variant
Chromosome / position
2:234854552
HGVS
NM_024080.5,c.752A>G,p.Tyr251Cys
Allele change
Missense_Y251C

Public references

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