Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2865531
CFDP1
1.000 0.040 16 75356418 intron variant T/A snv 0.52 3
rs2904259
FAM13A
4 88964563 intron variant T/A;C snv 3
rs7733088
HTR4 ; LOC107986462
1.000 0.040 5 148476770 intron variant G/A;C snv 0.44; 4.1E-06 3
rs17331332
INTS12
4 105886950 intron variant G/A snv 4.5E-02 3
rs1435867
LINC01807
2 228646213 intron variant T/C snv 7.3E-02 3
rs2045517
LOC105377327 ; FAM13A
4 88949813 intron variant C/T snv 0.49 3
rs2869966
LOC105377327 ; FAM13A
1.000 0.040 4 88947927 intron variant C/T snv 0.47 3
rs1828591
LOC105377462
1.000 0.040 4 144559628 intron variant A/G snv 0.43 3
rs11168048
LOC107986462 ; HTR4
5 148462790 intron variant T/C snv 0.38 3
rs11001819
LRMDA
10 76555466 intron variant G/A snv 0.41 3
rs12447804
MMP15
16 58041378 intron variant C/T snv 0.18 3
rs8192575
NOTCH4
1.000 0.120 6 32198607 intron variant C/G;T snv 7.0E-02; 4.1E-06 3
rs2856437
PBX2
1.000 0.120 6 32189587 intron variant G/A snv 3.7E-02 3
rs16909898
PTCH1 ; LOC100507346
9 95468726 intron variant A/G snv 8.4E-02 0.10 3
rs1529672
RARB
1.000 0.040 3 25479091 intron variant C/A;T snv 3
rs1036429
SNRPF ; CCDC38
12 95877650 intron variant T/C snv 0.79 3
rs12899618
THSD4
15 71352781 intron variant G/A snv 0.14 3
rs2571445
TNS1
0.925 0.080 2 217818431 missense variant A/G;T snv 0.62 3
rs10824425 10 76580552 intergenic variant G/C snv 0.42 2
rs12664563 6 142464064 intergenic variant A/G snv 0.21 2
rs1512288 1.000 0.040 4 144570129 intron variant G/A snv 0.42 2
rs1541374 4 105127203 intergenic variant T/A;G snv 2
rs155259 6 142525428 downstream gene variant G/A snv 0.39 2
rs16909856 9 95442211 downstream gene variant G/A;C;T snv 2
rs1928528 6 142457972 intergenic variant T/G snv 0.21 2