Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2075672
TFR2 ; ACTL6B
7 100642673 intron variant A/G snv 0.65 1
rs7149242 14 100693079 intergenic variant T/G snv 0.62 1
rs11628318 14 102573750 regulatory region variant T/A;C snv 1
rs2297067
EXOC3L4
1.000 0.080 14 103100448 missense variant C/T snv 0.22 0.20 2
rs944002
EXOC3L4
14 103106478 intron variant A/G snv 0.25 2
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 4
rs6993770
ZFPM2 ; ZFPM2-AS1
0.925 0.080 8 105569300 intron variant A/T snv 0.31 2
rs342275
CTB-30L5.1
7 106718770 intron variant C/T snv 0.33 1
rs342293
CTB-30L5.1
0.882 0.040 7 106731773 intron variant C/G snv 0.42 1
rs4766566
CUX2
0.851 0.200 12 111269073 intron variant C/T snv 0.42 2
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs739496
SH2B3 ; ATXN2
0.790 0.160 12 111449855 3 prime UTR variant A/G snv 0.27 3
rs6490294
ACAD10
12 111752634 intron variant C/A snv 0.35 1
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 4
rs17824620
RPH3A
12 112663189 intron variant C/A snv 0.26 1
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 6
rs4938642
CBL
1.000 0.040 11 119229196 intron variant G/C snv 6.0E-02 1
rs2336384
MFN2
1.000 0.040 1 11986006 intron variant G/T snv 0.65 1
rs7961894
WDR66
12 121927677 intron variant C/T snv 7.3E-02 2
rs7616006 3 12226148 intergenic variant A/G snv 0.48 1
rs3792366
PDIA5
3 123121029 intron variant G/A;T snv 1
rs4731120
HYAL4
7 123771169 intergenic variant A/C snv 6.5E-02 1
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 9
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 3
rs10058074
MIR3936HG
5 132350453 intron variant G/A snv 0.31 1