Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 5
rs11746443
RGS14
0.882 0.120 5 177371305 intron variant G/A snv 0.24 0.21 3
rs1000597 0.925 0.120 7 30897563 intron variant T/A;C snv 2
rs4142110
DGKH
0.925 0.120 13 42180386 intron variant T/C snv 0.34 2
rs12654812
RGS14
0.925 0.120 5 177367190 intron variant G/A snv 0.34 2
rs1014290
SLC2A9 ; LOC105374476
0.827 0.280 4 10000237 intron variant G/A snv 0.72 2
rs1256328
ALPL
0.925 0.120 1 21570274 intron variant C/T snv 0.16 0.14 1
rs1042636
CASR
0.672 0.360 3 122284922 missense variant A/G snv 0.15 9.0E-02 1
rs17251221
CASR
0.724 0.360 3 122274400 intron variant A/G snv 0.11 1
rs1801725
CASR
0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 1
rs7627468
CASR
1.000 0.120 3 122227252 intron variant A/G snv 0.74 1
rs219778
CLDN14 ; LOC105369301
0.925 0.120 21 36462343 intron variant A/G snv 0.31 1
rs5896
F2
0.882 0.160 11 46723453 missense variant C/G;T snv 0.21 1
rs12669187
INMT-MINDY4 ; MINDY4
0.925 0.120 7 30875863 intron variant G/A snv 7.2E-02 1
rs199565725
LOC105369301 ; CLDN14
1.000 0.120 21 36462941 intron variant CA/- delins 6.6E-02 1
rs219780
LOC105369301 ; CLDN14
0.925 0.120 21 36461009 synonymous variant C/A;T snv 4.0E-06; 0.16 1
rs219781
LOC105369301 ; CLDN14
1.000 0.120 21 36460323 non coding transcript exon variant G/T snv 0.25 1
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 1
rs737267
SLC2A9
0.851 0.240 4 9933120 intron variant G/A;T snv 1
rs6449213
SLC2A9 ; LOC105374476
0.827 0.240 4 9992591 intron variant C/T snv 0.82 1
rs4293393
UMOD
0.827 0.200 16 20353266 intron variant A/G snv 0.20 1
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 1