Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs998871
TBPL2
14 55451584 intron variant G/A snv 0.64 1
rs998259
GCH1
1.000 0.080 14 54888313 intron variant C/A;T snv 3
rs9919932
FBXO34
14 55347362 intron variant A/G snv 0.30 1
rs9919926
FBXO34
14 55347172 intron variant G/C snv 0.36 1
rs9919921 14 55228787 upstream gene variant A/G snv 0.26 1
rs9806061 14 55094412 intergenic variant C/T snv 0.17 1
rs9671895 14 55092944 intergenic variant T/C snv 0.31 1
rs9671455
GCH1
14 54862362 intron variant C/G;T snv 1
rs9671371
GCH1
14 54861917 intron variant C/T snv 0.34 1
rs9637599
PPM1K ; PPM1K-DT
4 88285078 intron variant A/C snv 0.56 3
rs946059
ATG14
14 55380748 intron variant A/G snv 0.57 1
rs946057
ATG14
14 55410680 intron variant A/T snv 0.44 1
rs945269 14 55739991 regulatory region variant G/A snv 0.35 1
rs943914
WDHD1
14 54973350 intron variant C/A snv 0.34 1
rs943912 14 54918609 regulatory region variant C/G snv 0.18 1
rs942317
KTN1-AS1
14 55557104 intron variant A/C snv 0.56 1
rs9411491 9 133280442 upstream gene variant T/C snv 0.18 2
rs9411488 9 133278802 upstream gene variant G/T snv 0.34 2
rs9323285
ATG14
14 55397111 intron variant C/A snv 0.30 1
rs9323283
ATG14
14 55374067 intron variant C/T snv 0.11 1
rs9323280
FBXO34
14 55334969 intron variant A/C snv 0.11 1
rs9323272 14 54822206 intergenic variant G/A;T snv 1
rs9285583
WDHD1
14 54964717 intron variant T/C snv 0.43 1
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 9
rs878521 7 44216044 downstream gene variant G/A snv 0.33 3