Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs45446698
CYP3A7-CYP3A51P ; CYP3A7 ; ZSCAN25
0.807 0.120 7 99735325 upstream gene variant T/G snv 2.7E-02 3
rs776746
CYP3A5 ; ZSCAN25
0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72 1
rs10273424
TMEM225B
0.925 0.080 7 99598450 intron variant T/A snv 0.13 1
rs10235235
ZNF394 ; ZNF789
0.925 0.080 7 99478208 intron variant T/C snv 0.13 1
rs1033602309
SHROOM2
1.000 0.080 X 9937279 missense variant G/C snv 1
rs8032477
IGF1R
0.851 0.200 15 98711325 intron variant C/A;T snv 2
rs1458028855
FARP1
1.000 0.080 13 98431278 missense variant G/A;T snv 5.2E-06; 5.2E-06 1
rs12285889 1.000 0.080 11 97291056 intergenic variant A/G snv 0.17 1
rs7308077
CFAP54
1.000 0.080 12 96514194 intron variant C/T snv 9.3E-02 1
rs17356907
PGAM1P5
0.925 0.080 12 95633983 intron variant A/G snv 0.28 3
rs780723017
MANEA
1.000 0.080 6 95606008 missense variant A/C;G snv 4.0E-06 1
rs757158
PON1
0.851 0.240 7 95326216 upstream gene variant C/T snv 0.58 1
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 3
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 4
rs17021918
PDLIM5
0.776 0.240 4 94641726 intron variant C/T snv 0.30 3
rs373540612
ABCA4
1.000 0.080 1 94098891 missense variant G/A snv 5.2E-05 2.8E-05 1
rs17262792
GRID2
1.000 0.080 4 92997722 intron variant T/C snv 9.1E-02 1
rs1111875 0.776 0.360 10 92703125 intergenic variant C/T snv 0.36 2
rs756245027
AKAP9
1.000 0.080 7 92096848 missense variant G/C snv 4.0E-06 1
rs542876370
SPTLC1
1.000 0.080 9 92055470 missense variant G/A snv 1.2E-05 7.0E-06 1
rs6964587
AKAP9
0.851 0.120 7 92001306 missense variant G/T snv 0.38 0.42 1
rs421379 0.925 0.080 5 91979496 intergenic variant T/C snv 0.75 1
rs10474352
ARRDC3-AS1
0.925 0.080 5 91436408 intron variant C/T snv 0.23 1
rs941764
CCDC88C
0.925 0.080 14 91374725 intron variant A/G snv 0.46 2
rs8042680
PRC1-AS1 ; PRC1
0.882 0.160 15 90978107 intron variant C/A snv 0.54 1