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: rs998871
rs998871
1 14 55451584 intron variant G/A snv 0.64 0.700 1.000 1 2012 2012
dbSNP: rs998259
rs998259
3 1.000 0.080 14 54888313 intron variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs9919932
rs9919932
1 14 55347362 intron variant A/G snv 0.30 0.700 1.000 1 2012 2012
dbSNP: rs9919926
rs9919926
1 14 55347172 intron variant G/C snv 0.36 0.700 1.000 1 2012 2012
dbSNP: rs9919921
rs9919921
1 14 55228787 upstream gene variant A/G snv 0.26 0.700 1.000 1 2012 2012
dbSNP: rs9806061
rs9806061
1 14 55094412 intergenic variant C/T snv 0.17 0.700 1.000 1 2012 2012
dbSNP: rs9671895
rs9671895
1 14 55092944 intergenic variant T/C snv 0.31 0.700 1.000 1 2012 2012
dbSNP: rs9671455
rs9671455
1 14 54862362 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs9671371
rs9671371
1 14 54861917 intron variant C/T snv 0.34 0.700 1.000 1 2012 2012
dbSNP: rs9637599
rs9637599
3 4 88285078 intron variant A/C snv 0.56 0.700 1.000 1 2016 2016
dbSNP: rs946059
rs946059
1 14 55380748 intron variant A/G snv 0.57 0.700 1.000 1 2012 2012
dbSNP: rs946057
rs946057
1 14 55410680 intron variant A/T snv 0.44 0.700 1.000 1 2012 2012
dbSNP: rs945269
rs945269
1 14 55739991 regulatory region variant G/A snv 0.35 0.700 1.000 1 2012 2012
dbSNP: rs943914
rs943914
1 14 54973350 intron variant C/A snv 0.34 0.700 1.000 1 2012 2012
dbSNP: rs943912
rs943912
1 14 54918609 regulatory region variant C/G snv 0.18 0.700 1.000 1 2012 2012
dbSNP: rs942317
rs942317
1 14 55557104 intron variant A/C snv 0.56 0.700 1.000 1 2012 2012
dbSNP: rs9411491
rs9411491
2 9 133280442 upstream gene variant T/C snv 0.18 0.700 1.000 1 2012 2012
dbSNP: rs9411488
rs9411488
2 9 133278802 upstream gene variant G/T snv 0.34 0.700 1.000 1 2012 2012
dbSNP: rs9323285
rs9323285
1 14 55397111 intron variant C/A snv 0.30 0.700 1.000 1 2012 2012
dbSNP: rs9323283
rs9323283
1 14 55374067 intron variant C/T snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs9323280
rs9323280
1 14 55334969 intron variant A/C snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs9323272
rs9323272
1 14 54822206 intergenic variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs9285583
rs9285583
1 14 54964717 intron variant T/C snv 0.43 0.700 1.000 1 2012 2012
dbSNP: rs9271366
rs9271366
9 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 0.700 1.000 1 2010 2010
dbSNP: rs878521
rs878521
3 7 44216044 downstream gene variant G/A snv 0.33 0.700 1.000 1 2016 2016