Variant (rsID / SNP)

rs868756

rs868756 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PUDP. The table records no clinical significance for this variant.

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Reference-table entries

PUDPNot classified

Variant type: missense_variant
HGVS: NM_001178135.2,c.593G>C,p.Cys198Ser
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.