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: rs11644601
rs11644601 		16 15078261 intron variant T/C snv 0.21
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018
dbSNP: rs11644601
rs11644601 		16 15078261 intron variant T/C snv 0.21
CUI: C0523744
Disease: Lipids measurement
Lipids measurement 		0.700 1.000 1 2016 2016
dbSNP: rs11644601
rs11644601 		16 15078261 intron variant T/C snv 0.21
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs11644601
rs11644601 		16 15078261 intron variant T/C snv 0.21
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2966157
rs2966157 		1.000 0.040 16 15062041 intron variant T/C snv 0.66
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs2966157
rs2966157 		1.000 0.040 16 15062041 intron variant T/C snv 0.66
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs4122352
rs4122352 		16 15080714 intron variant G/A snv 0.21
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012