Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs221774 0.851 0.080 7 100701361 upstream gene variant A/G;T snv 4
rs113473633
NFKB1
1.000 0.040 4 102527974 intron variant A/G snv 1.6E-02 4
rs28157
MACIR
1.000 0.040 5 103260136 intron variant G/C;T snv 1
rs12582330
C12orf42
1.000 0.040 12 103499163 upstream gene variant G/T snv 0.61 1
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 20
rs35074907
KEAP1
0.807 0.160 19 10489742 synonymous variant G/A snv 1.9E-02 1.5E-02 6
rs34678053
LOC112268138 ; IGHGP
1.000 0.040 14 105668934 non coding transcript exon variant G/A;C;T snv 1
rs11926659
CBLB
1.000 0.040 3 105780995 intron variant A/G snv 0.17 1
rs13090803 1.000 0.040 3 106216106 intron variant G/T snv 0.15 2
rs4293777
CLNK
0.925 0.080 4 10715315 intergenic variant G/A;C snv 2
rs17020055
VAV3
1.000 0.040 1 107793911 intron variant A/C snv 0.11 1
rs78495697
VAV3
1.000 0.040 1 107813097 intron variant C/T snv 9.2E-02 1
rs4915076
VAV3
0.882 0.080 1 107816883 intron variant T/C snv 9.1E-02 2
rs4915077
VAV3
1.000 0.040 1 107823394 intron variant T/C snv 9.0E-02 1
rs17020139
VAV3
1.000 0.040 1 107826861 intron variant G/A snv 9.0E-02 1
rs6798068
MYH15
1.000 0.040 3 108443515 intron variant G/A;C snv 1
rs484959 0.882 0.120 1 109823461 upstream gene variant T/A;C snv 2
rs11064860
C12orf76
1.000 0.040 12 110051403 intron variant C/T snv 0.18 1
rs9521838
RAB20
1.000 0.040 13 110553879 intron variant G/A snv 0.20 1
rs114378220
CAMK4
0.851 0.040 5 111230662 intron variant C/T snv 4.5E-02 5
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 7
rs597808
ATXN2
0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 10