Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800458
TTR
0.851 0.280 18 31592902 missense variant G/A snv 5.1E-02 5.2E-02 5
rs34203073
AGGF1
1.000 0.040 5 77035624 missense variant G/A snv 1.0E-02 9.9E-03 2
rs764821003
TGFBR2
3 30671823 missense variant G/A snv 1.4E-05 1
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs112735431
RNF213 ; RNF213-AS1
0.683 0.320 17 80385145 missense variant G/A;C snv 2.6E-04; 8.0E-06 24
rs759985000
BDNF
11 27700987 5 prime UTR variant G/A;C snv 4.2E-06; 8.4E-06 2
rs11591147
PCSK9
0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs1042579
THBD
0.732 0.240 20 23048087 missense variant G/A;T snv 0.19 16
rs387906853
SMAD3
0.925 0.040 15 67181297 stop gained G/A;T snv 3
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 16
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs2144151
ANGPT4
20 903001 intron variant T/G snv 0.40 1