Variant (rsID / SNP)

rs73440972

rs73440972 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PAQR5. Location: chromosome 15, position 69,652,451. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

PAQR5Not classified

Variant type: missense_variant
Chromosome / position: 15:69652451
HGVS: NM_001104554.2,c.32G>A,p.Ser11Asn
Allele change: Missense_S11N

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.