Variant (rsID / SNP)

rs140460765

rs140460765 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DPP6. Location: chromosome 7, position 154,645,534. Clinical significance in the table: Uncertain significance.

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Reference-table entries

DPP6Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 7:154645534
Cytoband: 7q36.2
HGVS: NM_130797.4(DPP6):c.1711A>C (p.Lys571Gln)
Allele change: Missense_K510Q

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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