Variant (rsID / SNP)
rs2970847
rs2970847 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PPARGC1A. Location: chromosome 4, position 23,815,924. The table records no clinical significance for this variant.
Reference-table entries
- Variant type
- synonymous_variant
- Chromosome / position
- 4:23815924
- HGVS
- NM_001330751.2,c.1197A>G,p.Thr399Thr
- Allele change
- Silent
Associated conditions / phenotypes
Type 2 Diabetes Mellitus|Hepatocellular Carcinoma|Diabetes Mellitus|Hypertrophic Cardiomyopathy|Body Mass Index Quantitative Trait Locus 11|Atrial Standstill 1|Body Mass Index Quantitative Trait Locus 18|Body Mass Index Quantitative Trait Locus 19|Body Mass Index Quantitative Trait Locus 10|Body Mass Index Quantitative Trait Locus 7|Body Mass Index Quantitative Trait Locus 4|Body Mass Index Quantitative Trait Locus 12|Muscle Hypertrophy|Multiple Sclerosis|Colorectal Cancer|Body Mass Index Quantitative Trait Locus 14|Body Mass Index Quantitative Trait Locus 9|Body Mass Index Quantitative Trait Locus 8
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.