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Variant (rsID / SNP)

rs201633413

PLEKHO2

rs201633413 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLEKHO2. Location: chromosome 15, position 65,134,221. The table records no clinical significance for this variant.

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Reference-table entries

PLEKHO2Not classified
Variant type
missense_variant
Chromosome / position
15:65134221
HGVS
NM_025201.5,c.6G>T,p.Glu2Asp
Allele change
Missense_E2D

Public references

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