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Variant (rsID / SNP)

rs9652588

PDILT

rs9652588 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PDILT. Location: chromosome 16, position 20,370,810. The table records no clinical significance for this variant.

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Reference-table entries

PDILTNot classified
Variant type
missense_variant
Chromosome / position
16:20370810
HGVS
NM_174924.2,c.1586G>A,p.Gly529Glu
Allele change
Missense_G529E

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.