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Variant (rsID / SNP)

rs3856806

PPARG

rs3856806 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PPARG. Location: chromosome 3, position 12,475,557. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

PPARGBenign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
3:12475557
Cytoband
3p25.2
HGVS
NM_138711.6(PPARG):c.1341C>T (p.His447=)
Allele change
Synonymous_H449H

Associated conditions / phenotypes

Glioma susceptibility 1|Diabetes Mellitus, Noninsulin-Dependent, with Acanthosis Nigricans and Hypertension|Obesity|PPARG-related familial partial lipodystrophy|PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR-GAMMA POLYMORPHISM

Public references

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