Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs603424
PKD2L1
1.000 0.080 10 100315722 intron variant G/A snv 0.34 13
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 12
rs12509595 1.000 0.080 4 80261400 intergenic variant T/C snv 0.23 10
rs10857147 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 9
rs13139571
LOC107984032 ; GUCY1A1
1.000 0.040 4 155724361 intron variant C/A snv 0.22 9
rs13389219
COBLL1
1.000 0.080 2 164672366 intron variant C/T snv 0.47 9
rs17367504
MTHFR
1.000 0.040 1 11802721 intron variant A/G snv 0.14 9
rs604723
ARHGAP42
1.000 0.040 11 100739815 intron variant T/C snv 0.78 9
rs17608766
LRRC37A2 ; GOSR2
1.000 0.040 17 46935905 3 prime UTR variant T/C snv 9.2E-02 8
rs9368222
CDKAL1
1.000 0.080 6 20686765 intron variant C/A;T snv 8
rs6021247
NFATC2
1.000 0.080 20 51492442 intron variant G/A snv 0.65 7
rs77924615
PDILT
1.000 0.080 16 20381010 intron variant G/A snv 0.16 7
rs1275988
KCNK3
1.000 0.080 2 26691496 upstream gene variant C/T snv 0.48 6
rs1530440
CABCOCO1
1.000 0.040 10 61764833 intron variant C/T snv 0.15 6
rs2067087
HOTTIP ; HOXA13
1.000 0.080 7 27202041 non coding transcript exon variant G/C;T snv 6
rs381815
PLEKHA7
1.000 0.040 11 16880721 intron variant C/A;T snv 0.24 6
rs4409766
BORCS7-ASMT ; BORCS7
1.000 0.040 10 102856906 intron variant T/C snv 0.14 6
rs6495122 1.000 0.040 15 74833304 downstream gene variant A/C snv 0.44 6
rs7209400
LOC102724596
1.000 0.040 17 49372695 intron variant C/T snv 0.47 6
rs76895963
CCND2-AS1 ; CCND2
1.000 0.080 12 4275678 intron variant T/G snv 1.5E-02 6
rs10184004 1.000 0.080 2 164651879 downstream gene variant C/T snv 0.48 5
rs11513729 1.000 0.080 12 111835695 downstream gene variant C/T snv 0.29 5
rs1250259
FN1 ; LOC105373868
1.000 0.040 2 215435759 missense variant T/A snv 0.76 0.79 5
rs2384550 1.000 0.040 12 114914926 regulatory region variant G/A snv 0.33 5
rs2823139 1.000 0.080 21 15204463 intron variant G/A snv 0.34 5