Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72681869
SOS2
14 50188639 missense variant G/A;C snv 4.0E-06; 4.1E-03 6
rs8068318
TBX2
17 61406405 non coding transcript exon variant C/T snv 0.56 6
rs9292468 5 32818967 intergenic variant T/A;C snv 6
rs932764
PLCE1
10 94136183 intron variant A/G snv 0.38 6
rs10184428 2 164155317 intron variant C/A;G snv 5
rs1126930
PRKAG1 ; DDN-AS1
12 49005349 missense variant G/C snv 2.1E-02 2.1E-02 5
rs11636952
LMAN1L
15 74821981 intron variant T/C snv 0.48 5
rs11725969
GUCY1A1
4 155705436 intron variant C/T snv 0.24 5
rs1173766 5 32804422 intergenic variant T/C snv 0.57 5
rs12258967
CACNB2
10 18439030 intron variant C/G;T snv 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
rs2004776
AGT
1 230712956 intron variant C/G;T snv 5
rs2013002 12 111762346 intron variant T/A;C snv 5
rs2249105
CEP68
2 65060762 intron variant A/G snv 0.40 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