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Variant (rsID / SNP)

rs61733127

PHLPP2

rs61733127 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PHLPP2. Location: chromosome 16, position 71,683,718. The table records no clinical significance for this variant.

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Reference-table entries

PHLPP2Not classified
Variant type
missense_variant
Chromosome / position
16:71683718
HGVS
NM_015020.3,c.3047T>C,p.Leu1016Ser
Allele change
Missense_L1016S

Public references

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