Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs347685
TFDP2
1.000 0.080 3 142088295 intron variant C/A snv 0.74 4
rs1066621 1.000 0.080 3 191708066 regulatory region variant C/T snv 0.39 2
rs12634709
LOC105377110
1.000 0.080 3 59603270 intron variant G/T snv 0.23 2
rs9846911 3 187500548 intergenic variant A/G snv 0.47 2
rs12721226
AGTR1
3 148741522 missense variant G/A snv 6.3E-04 1.6E-04 1
rs375411329
PPARG
3 12379746 missense variant A/G snv 7.0E-06 1
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs1126616
SPP1
0.827 0.280 4 87982701 synonymous variant C/G;T snv 0.32 0.26 8
rs734553
SLC2A9
0.851 0.240 4 9921380 intron variant G/A;T snv 7
rs17319721
SHROOM3
0.925 0.080 4 76447694 intron variant G/A snv 0.34 5
rs45539933
UCP1
0.882 0.280 4 140567914 missense variant C/T snv 8.7E-02 7.7E-02 5
rs1057518797
PKD2
4 88008090 frameshift variant CCCGGGCA/TAGGACG delins 3
rs2074379
ALPK1
1.000 4 112431743 missense variant G/A snv 0.62 0.65 3
rs2074388
ALPK1
1.000 4 112431241 missense variant G/A snv 0.62 0.65 3
rs2074380
ALPK1
4 112432155 missense variant G/A;T snv 8.5E-03; 2.4E-05 2
rs2074381
ALPK1
4 112432293 missense variant A/G snv 8.5E-03 5.5E-03 2
rs57802047 1.000 0.080 4 20645949 intergenic variant C/T snv 0.11 2
rs7660268 1.000 0.080 4 14348076 intergenic variant C/A snv 7.4E-02 2
rs78351985
C4orf54
4 99655532 upstream gene variant A/G snv 3.2E-04 1
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs11739136
KCNIP1 ; KCNMB1
0.827 0.200 5 170383792 missense variant C/T snv 9.9E-02 8.7E-02 10
rs373863828
CREBRF
0.851 0.160 5 173108771 missense variant G/A snv 4.0E-05 8.4E-05 6
rs6420094
SLC34A1
1.000 0.080 5 177390635 intron variant A/G snv 0.29 5
rs11959928
DAB2 ; C9
1.000 0.080 5 39397030 intron variant T/A snv 0.39 4