Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs758921595
MC5R
1.000 0.040 18 13826391 frameshift variant -/G ins 2.4E-05 2.8E-05 1
rs312262717
SPG11
0.790 0.240 15 44659104 frameshift variant A/-;AA delins 18
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs1176744
HTR3B
0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 19
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 16
rs11152369
TCF4
0.851 0.040 18 55399097 intron variant A/C snv 6.3E-02 5
rs7296288
DHH
0.851 0.080 12 49086185 upstream gene variant A/C snv 0.50 5
rs1054442
DDN
0.925 0.040 12 48995537 3 prime UTR variant A/C snv 0.46 4
rs17673138
NRG1
0.851 0.040 8 32840440 intron variant A/C snv 8.6E-02 4
rs137928907
STX2
0.882 0.040 12 130827204 missense variant A/C snv 1.4E-02 1.5E-02 3
rs1935062
DAOA ; DAOA-AS1
0.882 0.080 13 105475787 intron variant A/C snv 0.32 3
rs4380187 0.925 0.040 2 184947213 intergenic variant A/C snv 0.34 3
rs182107583
MMADHC-DT
0.925 0.080 2 149675023 intron variant A/C snv 4.2E-03 2
rs707467
PER3
0.925 0.120 1 7801624 intron variant A/C snv 0.22 2
rs73057489 0.925 0.080 12 17370820 regulatory region variant A/C snv 3.9E-02 2
rs11487077
NAPEPLD
1.000 0.040 7 103105631 intron variant A/C snv 6.5E-02 1
rs12275195
TENM4
1.000 0.040 11 79394755 intron variant A/C snv 0.12 1
rs17826395
ADCY2
1.000 0.040 5 7502943 intron variant A/C snv 0.16 1
rs4340844
CLOCK
1.000 0.040 4 55462689 intron variant A/C snv 0.33 1
rs6916861
FYN
1.000 0.040 6 111661054 3 prime UTR variant A/C snv 0.20 1
rs3751143
P2RX7 ; LOC105370032
0.742 0.480 12 121184501 missense variant A/C;G snv 0.19; 4.0E-06 12
rs12443954 0.851 0.040 16 89675088 intron variant A/C;G snv 5
rs17693963 0.882 0.040 6 27742386 upstream gene variant A/C;G snv 5
rs28456
FADS1 ; FADS2
0.925 0.120 11 61822009 intron variant A/C;G snv 5
rs878567
HTR1A
0.882 0.040 5 63960164 intron variant A/C;G snv 4