SLC15A1, solute carrier family 15 member 1, 6564

N. diseases: 31; N. variants: 4
Disease: Hypertriglyceridemia ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1289389
rs1289389 		13 98684036 3 prime UTR variant C/T snv 0.18
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		Nutritional and Metabolic Diseases 0.010 1.000 1 2019 2019
dbSNP: rs2297322
rs2297322 		1.000 0.040 13 98723927 missense variant C/G;T snv 0.22
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		Nutritional and Metabolic Diseases 0.010 1.000 1 2019 2019
dbSNP: rs4646234
rs4646234 		1.000 0.040 13 98684126 3 prime UTR variant T/C snv 0.11
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		Nutritional and Metabolic Diseases 0.010 1.000 1 2019 2019