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: rs2506030
rs2506030 		1 1.000 0.080 10 42952399 intergenic variant A/G snv 0.35 0.030 1.000 3 2015 2019
dbSNP: rs117617821
rs117617821 		2 0.925 0.080 7 84692873 intergenic variant T/C snv 2.6E-02 0.700 1.000 1 2018 2018
dbSNP: rs12428625
rs12428625 		2 0.925 0.080 13 86134644 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs12707682
rs12707682 		1 1.000 0.080 7 84814040 intergenic variant T/C snv 0.31 0.010 1.000 1 2016 2016
dbSNP: rs144432435
rs144432435 		2 0.925 0.080 10 43063942 intergenic variant C/T snv 1.2E-02 0.710 < 0.001 1 2018 2018
dbSNP: rs1583147
rs1583147 		1 1.000 0.080 7 84841891 regulatory region variant C/T snv 0.21 0.010 1.000 1 2016 2016
dbSNP: rs17653445
rs17653445 		2 0.925 0.080 10 37546726 downstream gene variant A/G snv 0.12 0.700 1.000 1 2018 2018
dbSNP: rs2435377
rs2435377 		1 1.000 0.080 10 43188152 downstream gene variant C/T snv 0.84 0.700 1.000 1 2009 2009
dbSNP: rs2505526
rs2505526 		1 1.000 0.080 10 43274443 intergenic variant A/G snv 0.12 0.700 1.000 1 2009 2009
dbSNP: rs2505994
rs2505994 		2 0.925 0.080 10 43073439 upstream gene variant T/C snv 0.81 0.700 1.000 1 2018 2018
dbSNP: rs2505995
rs2505995 		1 1.000 0.080 10 43074205 upstream gene variant A/G snv 0.43 0.700 1.000 1 2009 2009
dbSNP: rs3004214
rs3004214 		1 1.000 0.080 10 43136250 upstream gene variant C/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs4519046
rs4519046 		2 0.925 0.080 10 43379369 downstream gene variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs6509940
rs6509940 		2 0.925 0.080 19 55372511 upstream gene variant C/G;T snv 0.010 1.000 1 2015 2015
dbSNP: rs80227144
rs80227144 		2 0.925 0.080 7 84720526 regulatory region variant C/A snv 2.6E-02 0.700 1.000 1 2016 2016
dbSNP: rs8134637
rs8134637 		1 1.000 0.080 21 19758015 downstream gene variant T/C snv 3.0E-03 0.010 1.000 1 2018 2018
dbSNP: rs80068543
rs80068543
ARVCF
1 1.000 0.080 22 19981520 missense variant C/T snv 2.6E-02 2.4E-02 0.010 1.000 1 2017 2017
dbSNP: rs7785360
rs7785360
AUTS2
3 0.925 0.120 7 69944392 intron variant G/A snv 0.16 0.010 1.000 1 2018 2018
dbSNP: rs1447295
rs1447295
CASC8
29 0.658 0.400 8 127472793 intron variant A/C;T snv 0.010 1.000 1 2008 2008
dbSNP: rs6267
rs6267
COMT ; MIR4761
9 0.827 0.200 22 19962740 missense variant G/A;T snv 4.8E-05; 1.4E-02 0.010 1.000 1 2017 2017
dbSNP: rs2505506
rs2505506
CSGALNACT2
1 1.000 0.080 10 43150406 intron variant C/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs2054675
rs2054675
CYP2B6
1 1.000 0.080 19 40989850 upstream gene variant T/C snv 0.29 0.010 1.000 1 2015 2015
dbSNP: rs151128145
rs151128145
DNMT3B
1 1.000 0.080 20 32780396 missense variant G/A snv 7.7E-04 7.7E-04 0.010 1.000 1 2014 2014
dbSNP: rs61758433
rs61758433
DNMT3B
1 1.000 0.080 20 32787389 missense variant G/A;C;T snv 8.0E-06; 2.0E-05; 7.2E-05 0.010 1.000 1 2014 2014
dbSNP: rs2837770
rs2837770
DSCAM
1 1.000 0.080 21 40662426 intron variant G/A snv 0.34 0.010 1.000 1 2018 2018