Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11076962
RBFOX1
16 5761366 intron variant T/C snv 0.25 2
rs1107960 14 54917622 intergenic variant T/A snv 0.42 2
rs11265191
OR10J1 ; OR10J4
1 159430569 intron variant C/G;T snv 2
rs115024193
LOC105377299 ; BMP2K
4 78793500 intron variant T/A snv 2.3E-02 2
rs11588857
LRRN2 ; LOC105371692
1 204617919 missense variant G/A;T snv 0.20; 8.0E-06 2
rs11714441
ADCY5
3 123440099 intron variant C/T snv 0.40 2
rs11793831 9 23362313 intron variant G/A;T snv 2
rs118134876
THSD7A
7 11460745 missense variant C/A;T snv 4.0E-02 2
rs12028010 1 41298799 intron variant T/C snv 0.19 2
rs1223397
PHACTR1 ; TBC1D7 ; TBC1D7-LOC100130357
6 13270713 intron variant G/A;C snv 0.19 2
rs12446589
TUFM ; SH2B1
16 28859641 intron variant G/A snv 0.30 2
rs12761761
PPP2R2D
10 131961871 downstream gene variant C/T snv 0.21 2
rs12914495
DENND4A
15 65687454 intron variant A/G;T snv 2
rs13197257
PTPRK
6 128012537 intron variant G/T snv 0.21 2
rs13220261
LOC107986583 ; BTN1A1
6 26498957 upstream gene variant C/A;T snv 2
rs13259607 8 70439812 intergenic variant C/T snv 0.15 2
rs13428598
ARHGAP15
2 143492918 intron variant C/T snv 0.28 2
rs1343775 1 41292321 intron variant A/G snv 0.17 2
rs142601917 12 120914271 upstream gene variant C/A;G;T snv 2
rs1430055 2 16499521 intergenic variant G/A snv 0.61 2
rs143699161
LINC02210-CRHR1 ; LOC105371802
17 45671346 intron variant A/G snv 0.19 2
rs1473634 8 21057805 intron variant A/G snv 0.22 2
rs1492014 3 94352637 intergenic variant T/C;G snv 2
rs1582874
ZBTB38
3 141396377 5 prime UTR variant T/A;C snv 2
rs1614887
BTN2A2
6 26392793 synonymous variant G/A snv 0.53 0.63 2