Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs145475805
TG
0.882 0.080 8 132887509 missense variant A/G snv 8.8E-05 3.3E-04 4
rs7028661
PTCSC2
0.882 0.080 9 97776188 intron variant A/G snv 0.72 4
rs1031583860
GLYAT
0.882 0.080 11 58709815 missense variant T/C snv 3
rs1032006770
EGFR
0.882 0.080 7 55160171 missense variant A/G snv 4.0E-06 7.0E-06 3
rs10951937
SUN3
0.882 0.080 7 47992027 intron variant A/C snv 0.43 3
rs12769288
MGMT
0.882 0.080 10 129488086 intron variant C/T snv 0.10 3
rs1365943053
PTCH1
0.882 0.080 9 95516630 missense variant C/T snv 7.0E-06 3
rs180414
SLC38A4
0.882 0.080 12 46775115 synonymous variant A/G snv 3.1E-03 3
rs2145418 0.882 0.080 1 118422631 intergenic variant C/A snv 0.78 3
rs2708896
PKD1L1
0.882 0.080 7 47955186 upstream gene variant T/C;G snv 3
rs4658973
WDR3 ; SPAG17
0.882 0.080 1 117956431 intron variant T/G snv 0.34 3
rs7037324
LOC112268051
0.882 0.080 9 97896036 regulatory region variant A/G snv 0.71 3
rs709399
XRCC3 ; KLC1 ; LOC112268131
0.882 0.080 14 103701208 3 prime UTR variant G/A snv 0.59 0.61 3
rs747463591
CCDC6
0.882 0.080 10 59906391 missense variant C/A;G;T snv 4.9E-06; 9.9E-06 3
rs779791579
PTCH1
0.882 0.080 9 95508325 missense variant G/C snv 7.8E-04 6.1E-04 3
rs78929565
CLOCK
0.882 0.080 4 55539035 intron variant C/A;T snv 3
rs1418810723
FN1
0.851 0.080 2 215409981 missense variant A/T snv 8.0E-06 9
rs1064795638
BAP1
0.851 0.080 3 52403251 stop gained G/A snv 7
rs768827923
PIK3CD
0.851 0.080 1 9721816 missense variant T/G snv 6
rs776935407
SGSM3
0.851 0.080 22 40409261 missense variant T/A snv 4.1E-06 6
rs1248131654
RBMS1
0.851 0.080 2 160367217 missense variant G/A snv 1.4E-05 4
rs13143866
IL21 ; IL21-AS1
0.851 0.200 4 122619603 intron variant G/A snv 0.24 4
rs1443434
FOXE1
0.851 0.080 9 97855197 3 prime UTR variant G/T snv 0.63 4
rs1800858
RET
0.851 0.160 10 43100520 synonymous variant A/C;G snv 0.73 4
rs1946519
IL18
0.851 0.120 11 112164784 intron variant A/C snv 0.60 4