Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10414689
rs10414689 		2 19 51293045 regulatory region variant T/C snv 0.11 0.700 1.000 1 2013 2013
dbSNP: rs10518202
rs10518202 		1 4 78758523 intergenic variant G/T snv 9.6E-02 0.700 1.000 1 2018 2018
dbSNP: rs12529874
rs12529874 		2 6 98014625 intron variant G/A snv 2.6E-02 0.700 1.000 1 2013 2013
dbSNP: rs12623456
rs12623456 		2 2 163162632 intergenic variant T/C snv 2.2E-02 0.700 1.000 1 2017 2017
dbSNP: rs17003443
rs17003443 		1 4 78749373 TF binding site variant C/T snv 6.3E-02 0.700 1.000 1 2018 2018
dbSNP: rs17254590
rs17254590 		2 13 106384996 downstream gene variant G/C snv 2.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs17424324
rs17424324 		1 7 133111563 intergenic variant A/T snv 0.11 0.700 1.000 1 2017 2017
dbSNP: rs2581624
rs2581624 		2 3 142915027 intron variant G/C;T snv 0.29 0.700 1.000 1 2015 2015
dbSNP: rs3762220
rs3762220 		2 20 18797336 upstream gene variant G/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs4432766
rs4432766 		1 4 78751385 regulatory region variant T/A snv 0.17 0.700 1.000 1 2018 2018
dbSNP: rs62519907
rs62519907 		2 8 71696834 intron variant G/A;T snv 0.17 0.700 1.000 1 2019 2019
dbSNP: rs6722456
rs6722456 		2 2 133771520 intergenic variant G/A snv 4.5E-02 0.700 1.000 1 2013 2013
dbSNP: rs7160151
rs7160151 		2 14 49336446 intergenic variant A/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs742614
rs742614 		2 20 33894826 intergenic variant A/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs77164426
rs77164426 		2 2 146756888 intergenic variant A/G snv 1.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs994988
rs994988 		2 6 103351171 intergenic variant C/T snv 0.44 0.700 1.000 1 2013 2013
dbSNP: rs11083274
rs11083274
ABHD3
1 18 21677162 intron variant T/C snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs2391388
rs2391388
ALG14
2 1 95020269 intron variant A/C snv 0.49 0.700 1.000 1 2013 2013
dbSNP: rs6675668
rs6675668
ALG14
2 1 95050081 intron variant T/G snv 0.43 0.700 1.000 1 2013 2013
dbSNP: rs4770891
rs4770891
ATP8A2
1 13 25983588 intron variant C/G snv 8.0E-02 0.700 1.000 1 2018 2018
dbSNP: rs7335338
rs7335338
ATP8A2
1 13 25668367 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs12580543
rs12580543
C1S ; LPCAT3 ; EMG1
1 12 6992881 intron variant A/C snv 0.12 0.700 1.000 1 2015 2015
dbSNP: rs11120822
rs11120822
CAMTA1
2 1 7053052 intron variant G/C snv 0.34 0.700 1.000 1 2013 2013
dbSNP: rs1824965
rs1824965
CHAER1
1 4 56703381 intergenic variant T/C snv 0.50 0.700 1.000 1 2018 2018
dbSNP: rs16838623
rs16838623
CHRM3
2 1 239648090 intron variant A/C snv 3.4E-02 0.700 1.000 1 2017 2017