Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 4
rs1011970
CDKN2B-AS1
0.677 0.320 9 22062135 intron variant G/T snv 0.23 1
rs10146997
NRXN3
0.827 0.240 14 79478819 intron variant A/G snv 0.25 1
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
rs1038304
CCDC170 ; LOC107986528
0.882 0.160 6 151612040 intron variant A/G snv 0.58 1
rs1041981
LOC100287329 ; LTA
0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 2
rs1042031
APOB
0.790 0.200 2 21002881 stop gained C/A;T snv 8.0E-06; 0.15 3
rs10472076 0.925 0.080 5 58888234 regulatory region variant T/A;C snv 1
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 3
rs1053872
RCL1
0.925 0.080 9 4860643 3 prime UTR variant G/C;T snv 2
rs1058808
ERBB2
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 1
rs10736303
FGFR2
0.882 0.120 10 121574943 intron variant G/A snv 0.40 1
rs1075496
NRM
0.882 0.160 6 30690462 intron variant C/A snv 0.47 1
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 4
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
rs10811650
CDKN2B-AS1
0.882 0.200 9 22067594 intron variant A/G snv 0.37 4
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 4
rs10822013
ZNF365
0.851 0.080 10 62492218 intron variant C/T snv 0.42 1
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 2
rs10896449 0.827 0.200 11 69227200 intergenic variant A/G snv 0.53 2
rs10931936
CASP8
0.827 0.120 2 201279205 intron variant T/C snv 0.72 2