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Variant (rsID / SNP)

rs2269706

PPP1R18

rs2269706 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PPP1R18. Location: chromosome 6, position 30,652,872. The table records no clinical significance for this variant.

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Reference-table entries

PPP1R18Not classified
Variant type
synonymous_variant
Chromosome / position
6:30652872
HGVS
NM_001134870.2,c.924C>T,p.Ser308Ser
Allele change
Synonymous_S308S

Public references

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