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Variant (rsID / SNP)

rs61744951

PPL

rs61744951 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PPL. Location: chromosome 16, position 4,934,777. The table records no clinical significance for this variant.

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Reference-table entries

PPLNot classified
Variant type
synonymous_variant
Chromosome / position
16:4934777
HGVS
NM_002705.5,c.3879G>A,p.Gln1293Gln
Allele change
Synonymous_Q1293Q

Public references

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