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: rs1150660
rs1150660
5 0.925 0.120 6 26101212 upstream gene variant A/C snv 0.73 0.700 1.000 1 2009 2009
dbSNP: rs7671266
rs7671266
4 0.925 0.120 4 10054752 intron variant T/C snv 0.73 0.800 1.000 2 2009 2011
dbSNP: rs199726
rs199726
5 0.925 0.120 6 25953132 intergenic variant G/A snv 0.73 0.700 1.000 1 2009 2009
dbSNP: rs129129
rs129129
5 0.925 0.120 6 25960801 upstream gene variant A/G snv 0.73 0.700 1.000 1 2009 2009
dbSNP: rs1014290
rs1014290
6 0.827 0.280 4 10000237 intron variant G/A snv 0.72 0.700 1.000 1 2009 2009
dbSNP: rs442601
rs442601
5 0.925 0.120 6 25934296 upstream gene variant G/A snv 0.72 0.700 1.000 1 2009 2009
dbSNP: rs199736
rs199736
5 0.925 0.120 6 25936559 intergenic variant C/T snv 0.72 0.700 1.000 1 2009 2009
dbSNP: rs6853437
rs6853437
3 0.925 0.120 4 10003811 intron variant G/A snv 0.72 0.700 1.000 1 2009 2009
dbSNP: rs9291640
rs9291640
3 0.925 0.120 4 10005462 intron variant C/T snv 0.72 0.700 1.000 1 2009 2009
dbSNP: rs10022499
rs10022499
3 0.925 0.120 4 10004913 intron variant C/A snv 0.72 0.700 1.000 1 2009 2009
dbSNP: rs10023068
rs10023068
3 0.925 0.120 4 10003208 intron variant A/G snv 0.72 0.700 1.000 1 2009 2009
dbSNP: rs13241427
rs13241427
6 1.000 7 1249003 regulatory region variant G/T snv 0.72 0.700 1.000 1 2015 2015
dbSNP: rs3733588
rs3733588
3 0.925 0.120 4 9995679 non coding transcript exon variant G/A snv 0.72 0.700 1.000 2 2009 2011
dbSNP: rs4697954
rs4697954
3 0.925 0.120 4 10172905 regulatory region variant A/G snv 0.71 0.700 1.000 1 2009 2009
dbSNP: rs938555
rs938555
3 0.925 0.120 4 9924427 intron variant A/G snv 0.71 0.700 1.000 1 2009 2009
dbSNP: rs13125209
rs13125209
3 0.925 0.120 4 9980420 intron variant A/C snv 0.71 0.700 1.000 1 2009 2009
dbSNP: rs938554
rs938554
3 0.925 0.120 4 9924068 non coding transcript exon variant C/G snv 0.71 0.700 1.000 1 2009 2009
dbSNP: rs606458
rs606458
SF1
4 0.882 0.160 11 64778919 upstream gene variant C/A;T snv 0.71 0.700 1.000 1 2011 2011
dbSNP: rs3775947
rs3775947
1 4 9993616 intron variant C/T snv 0.71 0.700 1.000 1 2019 2019
dbSNP: rs7663032
rs7663032
3 0.925 0.120 4 9992214 intron variant C/G;T snv 0.71 0.700 1.000 2 2009 2011
dbSNP: rs4610325
rs4610325
3 0.925 0.120 4 10411544 non coding transcript exon variant T/C snv 0.71 0.700 1.000 1 2009 2009
dbSNP: rs1407040
rs1407040
4 20 58897119 intron variant C/T snv 0.70 0.700 1.000 1 2019 2019
dbSNP: rs16868246
rs16868246
3 0.925 0.120 4 9976681 intron variant C/G snv 0.70 0.700 1.000 1 2009 2009
dbSNP: rs11952102
rs11952102
1 5 177313703 upstream gene variant G/A snv 0.70 0.700 1.000 1 2019 2019
dbSNP: rs7697246
rs7697246
3 0.925 0.120 4 10407133 upstream gene variant C/T snv 0.70 0.700 1.000 1 2009 2009