Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10865879
EXOG
3 38535871 intron variant A/C snv 0.21 1
rs2242285
SLC25A26 ; LRIG1
3 66381178 intron variant A/C;G snv 2
rs1562782
CAND1.11 ; AMPD3
11 10321164 intron variant A/C;G snv 1
rs2051211
EXOG
3 38518258 intron variant A/C;G snv 0.23 1
rs6795970
SCN10A
0.807 0.200 3 38725184 missense variant A/G snv 0.65 0.70 13
rs12036340 1 162045950 intergenic variant A/G snv 0.24 2
rs13195040
ZNF184
1.000 0.040 6 27446145 downstream gene variant A/G snv 9.0E-02 2
rs1733724
LNCAROD
10 52464217 intron variant A/G snv 0.82 2
rs4687718
TKT
3 53248287 intron variant A/G snv 0.75 2
rs7784776 7 46580547 intergenic variant A/G snv 0.42 2
rs10488821
MPPED2
11 30480628 intron variant A/G snv 0.30 1
rs13314892
MITF
3 69745901 intron variant A/G snv 0.23 1
rs1419856 7 35267372 intergenic variant A/G snv 0.11 1
rs6683273
PRDM16
1 3342619 intron variant A/G snv 6.8E-02 1
rs7537765
CLCN6
1 11827246 intron variant A/G snv 0.15 0.18 1
rs7211246
NSRP1
17 30158744 intron variant A/G;T snv 1
rs11710077
SCN5A
3 38616408 intron variant A/T snv 0.17 3
rs11079159
HLF
17 55296189 intron variant A/T snv 0.25 1
rs1321311 0.742 0.160 6 36655123 regulatory region variant C/A snv 0.28 15
rs174577
FADS2
1.000 0.080 11 61837342 intron variant C/A snv 0.38 13
rs359466
CPEB4
5 173888863 5 prime UTR variant C/G snv 0.11 1
rs883079
TBX5
1.000 0.080 12 114355435 3 prime UTR variant C/G;T snv 1.8E-05; 0.61 3
rs728926
KLF12
13 73938985 intron variant C/T snv 0.34 2
rs9851724 3 38678444 intergenic variant C/T snv 0.73 2
rs991014
SETBP1
18 44859921 intron variant C/T snv 0.35 2