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Variant (rsID / SNP)

rs71238846

PLEKHM1

rs71238846 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLEKHM1. Location: chromosome 17, position 43,552,537. The table records no clinical significance for this variant.

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Reference-table entries

PLEKHM1Not classified
Variant type
synonymous_variant
Chromosome / position
17:43552537
HGVS
NM_014798.3,c.852C>T,p.Cys284Cys
Allele change
Synonymous_C284C

Public references

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