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: rs10457128
rs10457128 		1 6 105570101 intron variant G/A snv 0.65 0.700 1.000 1 2017 2017
dbSNP: rs10493718
rs10493718 		1 1 82597250 intron variant C/A snv 0.25 0.700 1.000 1 2017 2017
dbSNP: rs111913416
rs111913416
SORCS2
1 4 7706148 intron variant A/T snv 0.19 0.700 1.000 1 2017 2017
dbSNP: rs11225547
rs11225547 		1 11 103097123 upstream gene variant A/C snv 4.5E-02 0.700 1.000 1 2012 2012
dbSNP: rs11695685
rs11695685
CTNNA2
1 2 79695676 intron variant C/T snv 0.29 0.700 1.000 1 2008 2008
dbSNP: rs1211337
rs1211337
SUPT20H
1 13 37043162 intron variant G/A snv 7.9E-02 0.700 1.000 1 2012 2012
dbSNP: rs12279202
rs12279202
IPO7
2 11 9410543 intron variant C/T snv 4.8E-02 0.700 1.000 1 2012 2012
dbSNP: rs13201744
rs13201744 		1 6 6126612 intergenic variant C/A snv 8.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs140614282
rs140614282 		1 5 42918730 intron variant G/A snv 7.9E-03 0.700 1.000 1 2017 2017
dbSNP: rs143141511
rs143141511
SHROOM3
1 4 76647838 intron variant G/A snv 4.2E-03 0.700 1.000 1 2017 2017
dbSNP: rs16877320
rs16877320 		2 6 15922795 TF binding site variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs17054796
rs17054796
ALG5
1 13 36996594 intron variant T/C snv 7.8E-02 0.700 1.000 1 2012 2012
dbSNP: rs17365948
rs17365948
YWHAZ
2 8 100944649 intron variant C/T snv 4.0E-02 0.700 1.000 1 2012 2012
dbSNP: rs198284
rs198284
LOC107986777
1 7 24225724 intron variant C/T snv 0.94 0.700 1.000 1 2012 2012
dbSNP: rs2238776
rs2238776
TBX1
2 1.000 0.080 22 19770369 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs2375980
rs2375980 		3 9 2692622 intergenic variant C/G snv 0.51 0.700 1.000 1 2017 2017
dbSNP: rs282258
rs282258 		1 2 224050083 intergenic variant T/C snv 0.46 0.700 1.000 1 2017 2017
dbSNP: rs3025021
rs3025021
VEGFA
4 0.882 0.160 6 43781426 non coding transcript exon variant T/C snv 0.70 0.700 1.000 1 2017 2017
dbSNP: rs4349809
rs4349809 		2 6 43957093 intergenic variant T/A;G snv 0.700 1.000 1 2017 2017
dbSNP: rs4613079
rs4613079
CDYL2
2 16 80610060 intron variant G/A snv 4.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs465757
rs465757
MACROD2
1 20 15599638 intron variant G/A snv 0.60 0.700 1.000 1 2017 2017
dbSNP: rs6085948
rs6085948
LINC01428
1 20 7252703 intron variant G/A snv 0.60 0.700 1.000 1 2017 2017
dbSNP: rs7088799
rs7088799
JMJD1C
1 10 63256414 intron variant T/G snv 0.38 0.700 1.000 1 2017 2017
dbSNP: rs75885714
rs75885714
PLCL2
7 3 16901018 intron variant A/C snv 4.6E-02 0.700 1.000 1 2018 2018