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Variant (rsID / SNP)

rs2305535

DPP3

rs2305535 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DPP3. Location: chromosome 11, position 66,272,237. The table records no clinical significance for this variant.

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Reference-table entries

DPP3Not classified
Variant type
missense_variant
Chromosome / position
11:66272237
HGVS
NM_005700.5,c.2033G>A,p.Arg678His
Allele change
Missense_R648H

Public references

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