Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1033301
VSNL1
1.000 0.080 2 17592731 intron variant A/C snv 0.11 1
rs1036819
ZFAT-AS1 ; ZFAT
0.925 0.120 8 134599702 non coding transcript exon variant A/C snv 0.11 1
rs1408077
CR1
1.000 0.080 1 207630796 intron variant A/C snv 0.84 1
rs157590
TOMM40
0.882 0.160 19 44895459 intron variant A/C snv 0.60 1
rs17172199
HECW1
1.000 0.080 7 43337677 intron variant A/C snv 5.2E-02 1
rs2015475
MS4A4E ; MS4A4A
1.000 0.080 11 60231490 intron variant A/C snv 0.32 1
rs326946
ARHGAP20
1.000 0.080 11 110628530 intron variant A/C snv 0.26 1
rs4844610
CR1
1.000 0.080 1 207629207 intron variant A/C snv 0.87 1
rs714948
LOC107985305 ; CEACAM19 ; PVR
1.000 0.080 19 44662645 3 prime UTR variant A/C snv 0.92 1
rs75617873
PARVB
1.000 0.080 22 44130225 intron variant A/C snv 2.3E-02 1
rs7933202 1.000 0.080 11 60169453 downstream gene variant A/C snv 0.28 1
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 5
rs4147929
ABCA7
0.882 0.120 19 1063444 intron variant A/C;G snv 1
rs72832584
BCAS3
1.000 0.080 17 61215075 intron variant A/C;G snv 1
rs7521
MAPT ; KANSL1
0.925 0.080 17 46028029 3 prime UTR variant A/C;G snv 1
rs2965106 1.000 0.080 19 44729108 upstream gene variant A/C;G;T snv 1
rs387976
NECTIN2
1.000 0.080 19 44875803 intron variant A/C;T snv 4
rs10416371
NKPD1 ; LOC105372420 ; MARK4
1.000 0.080 19 45156878 intron variant A/C;T snv 1
rs11680911
LOC105373605
1.000 0.080 2 127131181 regulatory region variant A/C;T snv 1
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 15
rs2678379
APOB
1.000 0.080 2 21003688 intron variant A/G snv 0.76 7
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 6
rs6859
NECTIN2
0.827 0.120 19 44878777 3 prime UTR variant A/G snv 0.58 6
rs241448
TAP2
0.882 0.200 6 32828908 stop lost A/G snv 0.32 0.27 5