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: rs1032466
rs1032466
ATL1
1 1.000 0.120 14 50607743 intron variant A/C snv 0.27 0.700 1.000 1 2017 2017
dbSNP: rs4932194
rs4932194 		2 0.925 0.120 15 88702008 regulatory region variant A/C;G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs7524102
rs7524102 		5 0.882 0.160 1 22371954 intergenic variant A/G snv 0.21 0.700 1.000 2 2011 2017
dbSNP: rs10809650
rs10809650 		2 0.925 0.120 9 1202371 intergenic variant A/G snv 0.26 0.700 1.000 1 2011 2011
dbSNP: rs1509406
rs1509406
NEDD4
1 1.000 0.120 15 55937562 intron variant A/G snv 0.30 0.700 1.000 1 2017 2017
dbSNP: rs2179367
rs2179367 		2 0.925 0.120 6 149441401 regulatory region variant A/G snv 0.50 0.700 1.000 1 2011 2011
dbSNP: rs611744
rs611744
EIF3E
2 0.925 0.120 8 108215779 intron variant A/G;T snv 0.700 1.000 2 2011 2017
dbSNP: rs8124695
rs8124695 		2 0.925 0.120 20 40399796 intergenic variant C/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs16879765
rs16879765
SFRP4 ; EPDR1
2 0.925 0.120 7 37949493 intron variant C/T snv 0.13 0.700 1.000 2 2011 2017
dbSNP: rs10276303
rs10276303
LOC105375132
1 1.000 0.120 7 3279026 intron variant C/T snv 0.25 0.700 1.000 1 2017 2017
dbSNP: rs2306022
rs2306022
ITGA11
4 0.851 0.160 15 68335825 missense variant C/T snv 6.6E-02 5.8E-02 0.700 1.000 1 2017 2017
dbSNP: rs2598107
rs2598107
SFRP4 ; EPDR1
2 1.000 0.120 7 37933412 intron variant C/T snv 0.34 0.700 1.000 1 2017 2017
dbSNP: rs4730775
rs4730775
WNT2
4 0.851 0.200 7 117277064 3 prime UTR variant C/T snv 0.41 0.700 1.000 1 2011 2011
dbSNP: rs6016142
rs6016142 		3 1.000 0.120 20 39672165 intergenic variant C/T snv 7.8E-02 0.700 1.000 1 2017 2017
dbSNP: rs629535
rs629535
LINC01592
1 1.000 0.120 8 69095703 intron variant C/T snv 0.19 0.700 1.000 1 2017 2017
dbSNP: rs6496519
rs6496519 		1 1.000 0.120 15 88694953 intergenic variant C/T snv 0.16 0.700 1.000 1 2017 2017
dbSNP: rs7071275
rs7071275 		1 1.000 0.120 10 121662920 regulatory region variant C/T snv 0.19 0.700 1.000 1 2017 2017
dbSNP: rs7838717
rs7838717
BOP1
3 1.000 0.120 8 144280310 intron variant C/T snv 0.30 0.700 1.000 1 2017 2017
dbSNP: rs11672517
rs11672517
DUXA
2 0.925 0.120 19 57166826 intron variant G/A snv 0.24 0.700 1.000 2 2011 2017
dbSNP: rs2912522
rs2912522
LINC01592
2 0.925 0.120 8 69080145 intron variant G/A snv 0.73 0.700 1.000 2 2011 2017
dbSNP: rs10866846
rs10866846
EBF2
1 1.000 0.120 8 25988159 intron variant G/A snv 0.32 0.700 1.000 1 2017 2017
dbSNP: rs12342106
rs12342106 		1 1.000 0.120 9 1201156 regulatory region variant G/A snv 0.32 0.700 1.000 1 2017 2017
dbSNP: rs9525927
rs9525927 		2 0.925 0.160 13 44268367 regulatory region variant G/A snv 0.80 0.700 1.000 1 2017 2017
dbSNP: rs977987
rs977987
CHST6
1 1.000 0.120 16 75472695 3 prime UTR variant G/A snv 0.52 0.700 1.000 1 2017 2017
dbSNP: rs1042704
rs1042704
MMP14
1 1.000 0.120 14 22843385 missense variant G/A;C snv 0.16 0.700 1.000 1 2017 2017