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: rs1344852
rs1344852 		1 4 20182314 intergenic variant G/A;C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1562782
rs1562782
AMPD3 ; CAND1.11
1 11 10321164 intron variant A/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs2207790
rs2207790
NFIA
1 1 61432295 intron variant G/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs2242285
rs2242285
LRIG1 ; SLC25A26
2 3 66381178 intron variant A/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs7198919
rs7198919
LITAF
1 16 11595035 intron variant T/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs7211246
rs7211246
NSRP1
1 17 30158744 intron variant A/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs7342028
rs7342028
VTI1A
2 10 112719503 intron variant G/C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs883079
rs883079
TBX5
3 1.000 0.080 12 114355435 3 prime UTR variant C/G;T snv 1.8E-05; 0.61 0.700 1.000 1 2016 2016
dbSNP: rs9470361
rs9470361 		12 0.776 0.080 6 36655602 regulatory region variant G/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs9912468
rs9912468
PRKCA
3 17 66322239 intron variant G/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs17391905
rs17391905 		2 1 51080468 intergenic variant T/G snv 3.7E-02 0.700 1.000 1 2016 2016
dbSNP: rs7771320
rs7771320 		1 6 7502516 upstream gene variant T/C snv 5.4E-02 0.700 1.000 1 2016 2016
dbSNP: rs6683273
rs6683273
PRDM16
1 1 3342619 intron variant A/G snv 6.8E-02 0.700 1.000 1 2016 2016
dbSNP: rs11700980
rs11700980
N6AMT1
1 21 28781917 regulatory region variant T/C snv 8.7E-02 0.700 1.000 1 2016 2016
dbSNP: rs13195040
rs13195040
ZNF184
2 1.000 0.040 6 27446145 downstream gene variant A/G snv 9.0E-02 0.700 1.000 1 2016 2016
dbSNP: rs17608766
rs17608766
GOSR2 ; LRRC37A2
8 1.000 0.040 17 46935905 3 prime UTR variant T/C snv 9.2E-02 0.700 1.000 1 2016 2016
dbSNP: rs11708996
rs11708996
SCN5A
6 0.925 0.120 3 38592432 intron variant G/C snv 0.11 0.700 1.000 1 2016 2016
dbSNP: rs1419856
rs1419856 		1 7 35267372 intergenic variant A/G snv 0.11 0.700 1.000 1 2016 2016
dbSNP: rs1362212
rs1362212 		2 7 35265695 intergenic variant G/A snv 0.11 0.700 1.000 1 2016 2016
dbSNP: rs359466
rs359466
CPEB4
1 5 173888863 5 prime UTR variant C/G snv 0.11 0.700 1.000 1 2016 2016
dbSNP: rs12764182
rs12764182
LRMDA
1 10 76131488 intron variant T/G snv 0.16 0.700 1.000 1 2016 2016
dbSNP: rs11710077
rs11710077
SCN5A
3 3 38616408 intron variant A/T snv 0.17 0.700 1.000 1 2016 2016
dbSNP: rs7537765
rs7537765
CLCN6
1 1 11827246 intron variant A/G snv 0.15 0.18 0.700 1.000 1 2016 2016
dbSNP: rs3770770
rs3770770
STRN
1 2 36965723 intron variant C/T snv 0.18 0.700 1.000 1 2016 2016
dbSNP: rs17020136
rs17020136
HEATR5B
2 2 37020872 intron variant T/C snv 0.24 0.18 0.700 1.000 1 2016 2016