Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10036748
TNIP1
0.752 0.360 5 151078585 intron variant C/A;T snv 1
rs1003878
TSBP1-AS1 ; TSBP1
0.882 0.200 6 32332045 stop gained G/A snv 0.19 0.23 3
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 4
rs1012507
TNFSF4 ; LOC100506023
1.000 0.080 1 173250332 intergenic variant G/T snv 0.32 1
rs10156091
ICA1
1.000 0.080 7 8147464 intron variant T/C snv 0.86 1
rs10168266
STAT4
0.776 0.400 2 191071078 intron variant C/T snv 0.19 3
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70 1
rs10181656
STAT4
0.763 0.360 2 191105153 intron variant G/C snv 0.79 1
rs10239340
TNPO3
1.000 0.080 7 129028456 intron variant T/A;G snv 1
rs10276619 1.000 0.080 7 50273756 downstream gene variant G/A snv 0.59 1
rs10279821
TNPO3
1.000 0.080 7 129043493 intron variant T/A;C snv 1
rs103294 0.827 0.200 19 54293995 downstream gene variant T/C snv 0.82 3
rs1041981
LOC100287329 ; LTA
0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 2
rs1046089
PRRC2A
0.882 0.200 6 31635190 missense variant G/A snv 0.36 0.40 3
rs10466455
LOC102723568
1.000 0.080 11 34759389 intergenic variant T/C snv 0.39 1
rs10484399 0.851 0.240 6 27566749 intergenic variant A/G snv 5.4E-02 3
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 7
rs10489265
TNFSF4 ; LOC100506023
0.827 0.200 1 173266926 regulatory region variant A/C snv 0.21 1
rs10498070 0.925 0.080 2 219833404 intergenic variant A/C snv 0.39 1
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 2
rs10499197 0.925 0.080 6 137811379 intergenic variant T/G snv 2.4E-02 1
rs10516487
BANK1
0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 2
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 1
rs1077393
BAG6
0.882 0.200 6 31642752 non coding transcript exon variant A/G snv 0.44 3
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 4