Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs932764
PLCE1
10 94136183 intron variant A/G snv 0.38 6
rs10059884 5 32832368 regulatory region variant C/A;T snv 5
rs10184428 2 164155317 intron variant C/A;G snv 5
rs11725969
GUCY1A1
4 155705436 intron variant C/T snv 0.24 5
rs1173766 5 32804422 intergenic variant T/C snv 0.57 5
rs12940887
ZNF652
17 49325445 intron variant C/T snv 0.28 5
rs12978472
INSR
19 7257979 intron variant C/G;T snv 5
rs13082711 3 27496418 intergenic variant T/C snv 0.16 5
rs13209747 6 126794309 intron variant C/G;T snv 0.36 5
rs1573643
FURIN
15 90877743 intron variant T/C snv 0.33 5
rs167479
RGL3
19 11416089 missense variant T/A;C;G snv 5
rs16849225 2 164050310 intron variant C/T snv 0.19 5
rs16896398
SLC22A7
6 43294966 upstream gene variant A/T snv 0.42 5
rs1731249
KCNK3
2 26697157 intron variant T/A snv 0.48 5
rs1813353
CACNB2
10 18418519 intron variant T/C snv 0.29 5
rs1894400
FES
15 90885725 intron variant C/T snv 0.28 5
rs2004776
AGT
1 230712956 intron variant C/G;T snv 5
rs2013002 12 111762346 intron variant T/A;C snv 5
rs2282978
LOC112268009 ; CDK6
7 92635096 intron variant T/C snv 0.38 5
rs35441 12 115115310 intergenic variant C/T snv 0.40 5
rs35443 12 115115073 intergenic variant G/C snv 0.40 5
rs3790604
WNT2B
1 112504257 intron variant C/A snv 7.8E-02 5
rs4373814 10 18131043 intergenic variant G/C;T snv 5
rs438885 2 164195781 intron variant A/T snv 0.56 5
rs4590817
CABCOCO1
10 61707795 intron variant G/C snv 0.15 5