Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 24
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 10
rs4418728 10 93079967 downstream gene variant G/T snv 0.42 8
rs13108218
HGFAC
4 3442204 intron variant A/G;T snv 7
rs12777
MIR3936HG ; SLC22A4
5 132335969 synonymous variant C/G snv 3.1E-02 2.8E-02 6
rs1533988 7 1253374 intergenic variant A/T snv 0.59 6
rs17216707 20 54115823 intergenic variant T/C snv 0.17 6
rs11072567
NRG4
15 76006403 intron variant A/G snv 0.43 5
rs2068888 10 93079885 downstream gene variant G/A snv 0.42 5
rs6127099 20 54114863 intergenic variant A/T snv 0.28 5
rs1011731
DNM3 ; PIGC
1 172377408 intron variant G/A snv 0.46 4
rs128494
CLDN14 ; LOC105369301
21 36461960 intron variant T/C snv 0.72 4
rs1407040
GNAS
20 58897119 intron variant C/T snv 0.70 4
rs2337106
SMAD7
18 48934533 intron variant C/A;G snv 4
rs2453580
SLC47A1
17 19535008 non coding transcript exon variant T/C snv 0.37 4
rs2928148
INO80
15 41109352 intron variant G/A snv 0.44 4
rs34720381
PRRC2C
1 171486183 intron variant C/T snv 7.3E-02 4
rs4820323
MAFF ; PLA2G6
22 38203760 non coding transcript exon variant C/A;G;T snv 4
rs6026578
GNAS ; LOC101927932
20 58888417 5 prime UTR variant C/G snv 0.60 4
rs6440003
ZBTB38
3 141375367 intron variant G/A snv 0.54 4
rs6809651
ETV5
3 186096853 intron variant G/A snv 0.14 4
rs7832708
MSRA
8 10332530 intron variant C/T snv 0.49 4
rs10206899
ALMS1P1
2 73673773 intron variant T/C;G snv 0.21; 3.9E-05 3
rs10254101
PRKAG2
7 151718450 intron variant C/T snv 0.23 3
rs10265221
PRKAG2
7 151717243 intron variant T/A;C snv 3