Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6857
NECTIN2
0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 8
rs641153
CFB ; CYP21A2
0.790 0.160 6 31946403 missense variant G/A;T snv 9.6E-02; 4.1E-06 1
rs2269426
TNXB
0.807 0.280 6 32108722 intron variant G/A snv 0.35 8
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 7
rs2070895
LIPC ; ALDH1A2
0.807 0.120 15 58431740 intron variant G/A snv 0.33 5
rs11755724
RREB1
0.807 0.320 6 7118757 intron variant A/G;T snv 3
rs1329428
CFH
0.807 0.160 1 196733680 intron variant C/T snv 0.44 2
rs1410996
CFH
0.807 0.240 1 196727803 intron variant G/A snv 0.46 2
rs2072633
CFB ; CYP21A2 ; NELFE
0.807 0.320 6 31951801 3 prime UTR variant A/G snv 0.59 2
rs2588809
RAD51B
0.807 0.160 14 68193711 intron variant T/C snv 0.80 2
rs422951
NOTCH4
0.807 0.280 6 32220606 missense variant T/C snv 0.40 0.40 2
rs10033900
CFI
0.807 0.040 4 109737911 intron variant T/C snv 0.54 1
rs13278062
LOC389641 ; TNFRSF10A
0.807 0.200 8 23225458 non coding transcript exon variant G/A;C;T snv 1
rs943080
LOC107986598
0.807 0.040 6 43858890 TF binding site variant C/T snv 0.61 1
rs2043085
ALDH1A2
0.827 0.080 15 58388755 intron variant T/C snv 0.54 4
rs1063355
HLA-DQB1-AS1 ; HLA-DQB1
0.827 0.320 6 32659937 3 prime UTR variant T/G snv 0.56 2
rs10737680
CFH
0.827 0.080 1 196710325 intron variant A/C snv 0.44 2
rs6677604
CFH
0.827 0.200 1 196717788 intron variant G/A snv 0.23 2
rs3093077 0.827 0.200 1 159709846 upstream gene variant A/C;G;T snv 1
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 10
rs17231506
CETP
0.851 0.040 16 56960616 upstream gene variant C/G;T snv 0.28 5
rs12614
CYP21A2 ; CFB
0.851 0.160 6 31946402 missense variant C/G;T snv 4.1E-06; 0.12 1
rs13095226
COL8A1
0.851 0.040 3 99677428 intron variant T/C snv 9.5E-02 1
rs379489
CFH
0.851 0.200 1 196724321 intron variant A/G snv 0.65 1
rs429608
CYP21A2 ; SKIV2L
0.851 0.160 6 31962685 intron variant G/A snv 0.14 0.16 1