Variant (rsID / SNP)

rs1040499

rs1040499 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PTX4. Location: chromosome 16, position 1,538,363. The table records no clinical significance for this variant.

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Reference-table entries

PTX4Not classified

Variant type: missense_variant
Chromosome / position: 16:1538363
HGVS: NM_001013658.1,c.106G>T,p.Gly36Cys
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.