Variant (rsID / SNP)

rs2745103

rs2745103 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PTX4. Location: chromosome 16, position 1,538,464. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

PTX4Not classified

Variant type: missense_variant
Chromosome / position: 16:1538464
HGVS: NM_001013658.1,c.5G>A,p.Gly2Glu
Allele change: Silent

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.