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Variant (rsID / SNP)

rs7562391

PPIL3

rs7562391 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PPIL3. Location: chromosome 2, position 201,736,166. The table records no clinical significance for this variant.

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Reference-table entries

PPIL3Not classified
Variant type
missense_variant
Chromosome / position
2:201736166
HGVS
NM_032472.4,c.450T>G,p.Asp150Glu
Allele change
Missense_D150E

Public references

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