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
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 15
rs11072567
NRG4
15 76006403 intron variant A/G snv 0.43 5
rs62033406
FTO
16 53790314 intron variant A/G snv 0.33 5
rs79598313
KDF1
1 26958422 intron variant C/A;T snv 5
rs11204682
ENSA
1 150623061 intron variant G/A;T snv 4
rs11663816 18 60208994 intergenic variant T/C snv 0.20 4
rs1407040
GNAS
20 58897119 intron variant C/T snv 0.70 4
rs2453580
SLC47A1
17 19535008 non coding transcript exon variant T/C snv 0.37 4
rs6026578
GNAS ; LOC101927932
20 58888417 5 prime UTR variant C/G snv 0.60 4
rs60808706
KCNQ1
11 2836003 intron variant G/A snv 0.12 4
rs7752448
ZSCAN31
6 28333322 intron variant A/G snv 0.15 4
rs9302635
DHX38
16 72110275 intron variant T/C;G snv 4
rs11940694
KLB
4 39413373 intron variant A/G snv 0.57 3
rs143193096
IGF1R
15 98916098 missense variant G/A;C snv 8.4E-05; 4.0E-06 3
rs151134704
NFKB1 ; LOC105377347
4 102616435 splice region variant C/T snv 1.6E-04 9.1E-05 3
rs16856823
LRP2
2 169343942 intron variant A/T snv 4.6E-02 3
rs199592697
WNT7A
3 13854632 missense variant C/T snv 1.7E-04 1.1E-04 3
rs2867112 2 651349 intergenic variant T/G snv 0.18 3
rs35506085
IGF2 ; INS-IGF2 ; IGF2-AS
11 2144346 intron variant G/A snv 0.17 3
rs4686914
LOC107986166
3 187999752 intron variant C/T snv 0.27 3
rs4788815
LOC105371334
16 71600908 intergenic variant A/T snv 0.69 3
rs78946096
DNAJC13
3 132469319 intron variant A/G snv 3.8E-02 3
rs11084786
LINC01801
19 34791277 intron variant A/G snv 0.38 2
rs12134456
GON4L
1 155752715 intron variant C/G snv 0.26 2