Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs901630 6 98091643 intron variant C/T snv 0.32 3
rs974471
LOC102724934
14 29216122 intron variant G/A snv 0.74 3
rs9771228
PDE1C
7 32282884 intron variant T/C snv 0.39 3
rs9906944
IGF2BP1
17 49014058 intron variant C/G;T snv 3
rs10129426 14 103552118 upstream gene variant G/A snv 0.54 2
rs10192369 2 160524377 intergenic variant G/A snv 0.45 2
rs10236197
PDE1C
7 32252149 intron variant T/C snv 0.41 2
rs1043595
CALU
7 128769958 3 prime UTR variant G/A snv 0.19 2
rs1046953
SEMA3F
3 50159664 synonymous variant C/T snv 0.41 0.39 2
rs10514301
LINC00461
5 88643836 intron variant C/T snv 0.16 2
rs10514303
MEF2C
5 88749212 intron variant C/A;G snv 6.1E-02 2
rs10783018
LOC101928219 ; LINC02607
1 95782279 non coding transcript exon variant G/A snv 0.74 2
rs10872224 6 97987249 intron variant G/T snv 0.67 2
rs10922907 1 90727492 downstream gene variant A/G;T snv 2
rs10949662
PTPRN2
7 157741413 intron variant C/A;T snv 2
rs1106761 8 141609134 intron variant G/A snv 0.28 2
rs11076962
RBFOX1
16 5761366 intron variant T/C snv 0.25 2
rs11079849
IGF2BP1
17 49013423 intron variant C/T snv 0.28 2
rs1108842
GNL3 ; PBRM1
3 52686064 5 prime UTR variant A/C;G;T snv 0.49; 4.0E-06 2
rs11209943
LOC105378797
1 72284817 intron variant A/G snv 0.53 2
rs1144
SRPK2
7 105115908 intron variant T/C snv 0.31 2
rs11588857
LRRN2 ; LOC105371692
1 204617919 missense variant G/A;T snv 0.20; 8.0E-06 2
rs11605348
NDUFS3 ; FAM180B
11 47584931 upstream gene variant G/A snv 0.28 2
rs11665567
KCNG2
18 79803334 intron variant G/A snv 0.18 2
rs11793831 9 23362313 intron variant G/A;T snv 2