Variant (rsID / SNP)

rs2946385

rs2946385 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PPARGC1A. Location: chromosome 4, position 23,886,323. The table records no clinical significance for this variant.

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Reference-table entries

PPARGC1ANot classified

Variant type: synonymous_variant
Chromosome / position: 4:23886323
HGVS: NM_001354828.2,c.286C>A,p.Arg96Arg
Allele change: Silent

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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