Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1003897973
LOC107985302 ; TRIP10
0.882 0.080 19 6746039 missense variant C/G snv 3
rs1007541
FSHR
0.882 0.080 2 48981895 intron variant C/T snv 0.16 4
rs1030389
SNHG14 ; PWAR6
0.882 0.080 15 25032641 non coding transcript exon variant A/G snv 0.41 3
rs1041981
LOC100287329 ; LTA
0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 25
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs10426502
MYDGF ; TNFAIP8L1
0.882 0.080 19 4651257 intron variant G/A snv 6.8E-02 3
rs1042725
HMGA2
0.882 0.080 12 65964567 3 prime UTR variant C/T snv 0.48 7
rs1045935
PWAR6 ; SNHG14
0.882 0.080 15 25036439 non coding transcript exon variant G/A;T snv 3
rs1047840
EXO1
0.708 0.280 1 241878999 missense variant G/A snv 0.36 0.40 19
rs1048512
PIGM ; KCNJ10
0.882 0.080 1 160025108 3 prime UTR variant G/A;T snv 0.13 3
rs1048638
CA9
0.807 0.160 9 35681125 3 prime UTR variant C/A;G snv 10
rs104886003
PIK3CA
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs1049216
CASP3
0.790 0.200 4 184628935 3 prime UTR variant A/G snv 0.27 9
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1058808
ERBB2
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs1059234
CDKN1A
0.790 0.120 6 36685820 3 prime UTR variant C/T snv 0.15 0.13 10
rs1060555
TNFAIP8L1 ; MYDGF
0.882 0.080 19 4652810 3 prime UTR variant C/G;T snv 3
rs10802996
EXO1
0.882 0.080 1 241847325 upstream gene variant C/A;G snv 5
rs10815144
JAK2 ; INSL6
0.882 0.080 9 5010192 intron variant G/A snv 0.62 3
rs10893506
ST3GAL4
0.882 0.080 11 126406065 5 prime UTR variant T/A;C snv 6.4E-06; 0.41 5
rs11064
TNFAIP8
0.807 0.120 5 119393693 3 prime UTR variant A/G snv 0.27 9
rs11079454
BRIP1
0.882 0.080 17 61679808 3 prime UTR variant T/A;C snv 3
rs1110839
PAX8-AS1 ; PAX8
0.807 0.120 2 113236840 non coding transcript exon variant G/A;C;T snv 6
rs11125
LGALS3
0.851 0.120 14 55145121 missense variant A/T snv 6.5E-02 5.7E-02 5