Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104895564
NLRP12
0.925 0.200 19 53810809 stop gained G/A snv 1.5E-04 4.3E-04 3
rs1050450
GPX1
0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs10507391
ALOX5AP
0.776 0.320 13 30737959 intron variant A/T snv 0.52 10
rs10507875
OBI1-AS1 ; EDNRB
0.925 0.160 13 77943119 intron variant A/G snv 0.17 3
rs1051931
PLA2G7
0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs1052053
PMF1 ; PMF1-BGLAP
1.000 0.080 1 156232382 missense variant A/C;G snv 1.0E-03; 0.38 3
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1052700
PLIN1 ; KIF7
1.000 0.040 15 89665079 3 prime UTR variant A/T snv 0.26 3
rs1057910
CYP2C9
0.776 0.280 10 94981296 missense variant A/C;G snv 6.3E-02; 4.0E-06 12
rs10743980
LRP6
0.882 0.120 12 12259861 intron variant T/A;C;G snv 4
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs10848683
CACNA1C-AS1 ; CACNA1C
12 2681964 missense variant C/T snv 4.0E-06; 0.78 0.71 1
rs10887800
LOC101929727 ; RNLS
0.790 0.280 10 88316086 intron variant A/G;T snv 11
rs10890917 11 108988857 intergenic variant C/A;G snv 3.5E-02 1
rs10947803
KCNK17
1.000 0.080 6 39302834 intron variant C/A snv 2
rs10958409 1.000 0.080 8 54414531 intergenic variant G/A snv 0.18 2
rs10988134
KYAT1 ; SPOUT1
0.925 0.080 9 128833128 3 prime UTR variant C/T snv 0.34 4
rs11030119
BDNF
11 27706555 intron variant G/A;T snv 3
rs11044400 12 19033113 intergenic variant C/T snv 0.13 1
rs11053646
OLR1
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 17
rs11066001
BRAP
0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 15
rs11072518 15 74942269 upstream gene variant T/A;C snv 3
rs11172113
LRP1
0.882 0.080 12 57133500 intron variant T/C snv 0.42 10