RS114782902 AGPAT2

Health Risk Chr 9:136677093 snv missense variant
Upload your DNA to see your genotype for this variant.
Associated Conditions
Monogenic diabetes
Congenital generalized lipodystrophy type 1
AGPAT2-related disorder
Monogenic diabetes
Congenital generalized lipodystrophy type 1
AGPAT2-related disorder
Population Frequencies
gnomAD ALL
0%
1kG AFR
1.1%
1kG ALL
99.7%
1kG AMR
100%
1kG EAS
100%
1kG EUR
100%
1kG SAS
100%
Other Variants in AGPAT2
rs104894093 rs116807569 rs387906355 rs104894100 rs121908925 rs606231168 rs121908926 rs797045222 rs142176861 rs886043265
Ask Dr. Hemsworth about this variant