Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1004446
IGF2 ; INS-IGF2 ; IGF2-AS
0.827 0.240 11 2148913 intron variant G/A snv 0.37 1
rs10045431 0.851 0.240 5 159387525 intron variant A/C snv 0.78 1
rs1014486
IL12A-AS1
1.000 0.080 3 159973324 intron variant T/C snv 0.39 1
rs10201872
SP140
1.000 0.080 2 230242009 intron variant C/T snv 0.13 1
rs1021156
LOC105375911
1.000 0.080 8 78663569 intron variant T/C snv 0.64 1
rs1036207
NDFIP1
1.000 0.080 5 142119476 intron variant A/G;T snv 3
rs10411936
EPS15L1
1.000 0.080 19 16437564 intron variant A/G snv 0.63 2
rs10466829
CLECL1
1.000 0.080 12 9723495 intron variant G/A snv 0.55 1
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 7
rs10492972
KIF1B
1.000 0.080 1 10293054 intron variant T/C snv 0.32 1
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 1
rs10500264 1.000 0.080 19 33259408 intergenic variant G/A snv 0.14 1
rs10509540
LOC101929727 ; RNLS
0.925 0.160 10 88263276 upstream gene variant T/C snv 0.25 1
rs10516487
BANK1
0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 1
rs10517086
LINC02357
0.882 0.160 4 26083889 intron variant G/A snv 0.27 1
rs1052553
MAPT
0.827 0.200 17 45996523 synonymous variant A/G snv 0.14 0.15 1
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 5
rs1064395
NCAN
0.882 0.120 19 19250926 3 prime UTR variant G/A snv 0.24 1
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 3
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 1
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 6
rs1077667
TNFSF14
0.925 0.120 19 6668961 intron variant C/G;T snv 1
rs10797431
LOC100996583
0.851 0.080 1 2569783 non coding transcript exon variant G/T snv 0.42 5
rs10800309 0.925 0.120 1 161502368 upstream gene variant A/G;T snv 2
rs10806425
BACH2
0.851 0.280 6 90216893 intron variant C/A snv 0.33 2