RS659366 UCP2

Health Risk Chr 11:73983708 snv non coding transcript exon variant
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What This Variant Does
"Data-mining analysis suggests an epigenetic pathogenesis for type 2 diabetes. Genetic prediction of ...
Associated Conditions
Population Frequencies
1kG AFR
45.4%
1kG ALL
40.9%
1kG AMR
57.6%
1kG EAS
57.9%
1kG EUR
63.5%
1kG SAS
37.1%
Other Variants in UCP2
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