Variant (rsID / SNP)

rs13631

rs13631 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DPP7. Location: chromosome 9, position 140,006,202. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

DPP7Not classified

Variant type: synonymous_variant
Chromosome / position: 9:140006202
HGVS: NM_013379.3,c.1212C>T,p.Leu404Leu
Allele change: Synonymous_L404L

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.