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Variant (rsID / SNP)

rs7417616

OR2T6

rs7417616 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR2T6. Location: chromosome 1, position 248,550,970. The table records no clinical significance for this variant.

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Reference-table entries

OR2T6Not classified
Variant type
missense_variant
Chromosome / position
1:248550970
HGVS
NM_001005471.2,c.61A>G,p.Asn21Asp
Allele change
Missense_N21D

Public references

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