Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519854
FGFR2
0.882 0.080 10 121488063 missense variant A/T snv 7
rs121913476
FGFR2
0.851 0.080 10 121498520 missense variant A/C;T snv 7
rs34670419
ZKSCAN5
1.000 0.080 7 99533211 3 prime UTR variant G/A;T snv 7.7E-06; 2.6E-02 7
rs786205228
PPP2R1A
0.827 0.080 19 52212718 missense variant C/G;T snv 6
rs11196418
CASP7
0.925 0.080 10 113678707 upstream gene variant G/A snv 0.11 4
rs117039649
MDM2
0.925 0.080 12 68808776 intron variant G/C snv 2.3E-02 4
rs149308960
ESR1
0.925 0.080 6 151842622 missense variant G/A;C;T snv 4.0E-06; 4.0E-06; 1.6E-03 4
rs1694964
LINC02025
0.925 0.080 3 84885341 intron variant G/T snv 4
rs8135424
CHEK2
0.925 0.080 22 28689804 intron variant G/A snv 0.14 4
rs1045242
TNFAIP8
0.925 0.080 5 119393632 3 prime UTR variant A/G snv 0.32 3
rs1156807933
MAX ; LOC100506321
0.925 0.080 14 65093799 missense variant T/C snv 4.0E-06 3
rs12112075
OGDH
0.925 0.080 7 44609201 intron variant G/A snv 1.8E-02 3
rs12934561
IL32
0.882 0.080 16 3068864 intron variant T/C snv 0.57 3
rs1451539938
CD82
0.925 0.080 11 44618361 missense variant A/G snv 4.1E-06 7.0E-06 3
rs17601876
MIR4713HG ; CYP19A1
1.000 0.080 15 51261712 intron variant A/G snv 0.58 3
rs2453839
IGFBP3
0.925 0.080 7 45913974 intron variant T/C snv 0.26 3
rs2475335
PTPRD
0.882 0.080 9 10260263 intron variant C/A;T snv 3
rs4980524
STIP1
0.882 0.080 11 64191787 intron variant A/C;T snv 3
rs937213
EIF2AK4
1.000 0.080 15 40029923 intron variant T/C snv 0.31 3
rs10502289
ENOSF1
0.925 0.080 18 676789 intron variant A/T snv 0.15 2
rs10733710
TGFBR1
0.925 0.080 9 99145142 intron variant G/A snv 0.21 2
rs11196445
CASP7
0.925 0.080 10 113710131 intron variant G/A snv 0.11 2
rs11224561
PGR
0.925 0.080 11 101034325 3 prime UTR variant C/A;T snv 2
rs11263761
HNF1B
1.000 0.080 17 37737784 intron variant A/G snv 0.44 2
rs1156920296
LOC108783645 ; HFE
0.925 0.080 6 26092918 missense variant G/A snv 2