Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1800764
rs1800764 		0.790 0.320 17 63473168 upstream gene variant C/G;T snv
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.020 1.000 2 2014 2014
dbSNP: rs1041536
rs1041536 		1.000 0.040 20 9907627 intergenic variant T/C snv 0.46
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.700 1.000 1 2015 2015
dbSNP: rs10447760
rs10447760 		0.851 0.040 7 114083210 upstream gene variant C/T snv 0.17
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.010 < 0.001 1 2019 2019
dbSNP: rs112961612
rs112961612 		1.000 0.040 20 41872026 intergenic variant T/A snv 8.2E-02
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.700 1.000 1 2019 2019
dbSNP: rs113793030
rs113793030 		1.000 0.040 10 70287104 upstream gene variant T/C snv 1.7E-02
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.700 1.000 1 2015 2015
dbSNP: rs115700680
rs115700680 		1.000 0.040 1 171381070 intergenic variant T/G snv 1.9E-02
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.700 1.000 1 2015 2015
dbSNP: rs1157659
rs1157659 		1.000 0.040 11 27736075 intron variant A/G snv 0.37
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.010 1.000 1 2013 2013
dbSNP: rs116065238
rs116065238 		1.000 0.040 1 171482283 upstream gene variant A/G snv 4.3E-03
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.700 1.000 1 2015 2015
dbSNP: rs116237496
rs116237496 		1.000 0.040 8 101033687 upstream gene variant T/C snv 4.0E-02
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.700 1.000 1 2015 2015
dbSNP: rs117070989
rs117070989 		1.000 0.040 6 137490510 downstream gene variant C/A snv 8.3E-03
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.700 1.000 1 2015 2015
dbSNP: rs117129097
rs117129097 		1.000 0.040 12 128054737 intron variant C/G;T snv 1.9E-03
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.010 1.000 1 2019 2019
dbSNP: rs117224174
rs117224174 		1.000 0.040 6 114654261 intergenic variant G/A snv 2.2E-02
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.700 1.000 1 2015 2015
dbSNP: rs1187120
rs1187120 		0.925 0.040 6 34182850 intergenic variant T/C snv 0.99
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.010 1.000 1 2015 2015
dbSNP: rs12230170
rs12230170 		1.000 0.040 12 128762838 intergenic variant T/A;G snv
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.700 1.000 1 2015 2015
dbSNP: rs12435940
rs12435940 		1.000 0.040 14 25552779 intergenic variant A/G snv 0.97
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.700 1.000 1 2015 2015
dbSNP: rs12468965
rs12468965 		1.000 0.040 2 53528621 downstream gene variant G/A snv 1.8E-02
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.700 1.000 1 2015 2015
dbSNP: rs138901640
rs138901640 		1.000 0.040 9 118031487 intron variant A/G snv 5.5E-03
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.700 1.000 1 2015 2015
dbSNP: rs139660738
rs139660738 		1.000 0.040 12 94791412 intergenic variant T/C snv 6.3E-03
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.700 1.000 1 2015 2015
dbSNP: rs141480664
rs141480664 		1.000 0.040 7 4469958 regulatory region variant G/A snv 1.0E-02
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.700 1.000 1 2015 2015
dbSNP: rs142609537
rs142609537 		1.000 0.040 15 95675665 intron variant A/G snv 1.8E-02
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.700 1.000 1 2015 2015
dbSNP: rs146594485
rs146594485 		1.000 0.040 20 3776090 downstream gene variant G/A snv 6.1E-03
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.700 1.000 1 2015 2015
dbSNP: rs149969998
rs149969998 		1.000 0.040 17 13692262 intergenic variant G/C;T snv
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.700 1.000 1 2015 2015
dbSNP: rs150418526
rs150418526 		1.000 0.040 17 38697587 upstream gene variant C/G;T snv
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.700 1.000 1 2015 2015
dbSNP: rs150616616
rs150616616 		1.000 0.040 5 121366663 downstream gene variant C/G;T snv
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.700 1.000 1 2015 2015
dbSNP: rs150759334
rs150759334 		1.000 0.040 4 60800528 downstream gene variant T/C snv 9.4E-03
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.700 1.000 1 2015 2015