Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1053872
RCL1
0.925 0.080 9 4860643 3 prime UTR variant G/C;T snv 2
rs10995190
ZNF365
0.882 0.080 10 62518923 intron variant G/A snv 0.16 2
rs1570669
CYP24A1
0.925 0.080 20 54157888 intron variant A/G snv 0.42 2
rs17356907
PGAM1P5
0.925 0.080 12 95633983 intron variant A/G snv 0.28 2
rs4849887 0.807 0.080 2 120487546 intergenic variant T/A;C snv 2
rs10235235
ZNF394 ; ZNF789
0.925 0.080 7 99478208 intron variant T/C snv 0.13 1
rs10273424
TMEM225B
0.925 0.080 7 99598450 intron variant T/A snv 0.13 1
rs1028842
RAD51B
1.000 0.080 14 68205006 intron variant C/A snv 0.17 1
rs10472076 0.925 0.080 5 58888234 regulatory region variant T/A;C snv 1
rs10759243 0.925 0.080 9 107543834 upstream gene variant C/A;T snv 1
rs10771399 0.827 0.080 12 28002147 intergenic variant A/G snv 8.9E-02 1
rs1079866 0.925 0.080 7 41430495 intergenic variant C/G snv 0.13 1
rs10822013
ZNF365
0.851 0.080 10 62492218 intron variant C/T snv 0.42 1
rs11075995
FTO
0.882 0.080 16 53821379 intron variant A/T snv 0.77 1
rs11196174
TCF7L2
1.000 0.080 10 112974337 intron variant A/C;G snv 1
rs11199914 0.925 0.080 10 121334387 intergenic variant C/T snv 0.40 1
rs11242675 0.925 0.080 6 1318643 downstream gene variant C/T snv 0.58 1
rs11552449
AP4B1 ; DCLRE1B
0.925 0.080 1 113905767 missense variant C/G;T snv 0.22 0.15 1
rs116264287
RAD51B
1.000 0.080 14 68221985 intron variant C/T snv 1
rs117351774
RAD51B
1.000 0.080 14 68221922 intron variant T/C snv 0.18 1
rs11780156
PVT1
0.925 0.080 8 128182395 intron variant C/T snv 0.13 1
rs11814448 0.925 0.080 10 22026914 intergenic variant A/C snv 0.21 1
rs11820646 0.925 0.080 11 129591276 upstream gene variant T/C;G snv 1
rs12422552 0.925 0.080 12 14260997 regulatory region variant G/C snv 0.30 1
rs12493607
TGFBR2
0.882 0.080 3 30641447 intron variant G/C;T snv 1