Variant (rsID / SNP)

rs1288386

rs1288386 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PODN. Location: chromosome 1, position 53,535,478. The table records no clinical significance for this variant.

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Reference-table entries

PODNNot classified

Variant type: 5_prime_UTR_variant
Chromosome / position: 1:53535478
HGVS: NM_001199080.4,c.-50G>A
Allele change: Missense_R32H

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.