Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7588550
ERBB4
0.851 0.160 2 212304043 intron variant G/A snv 0.96 4
rs12717111
CNDP2
1.000 0.080 18 74522015 3 prime UTR variant C/A snv 0.95 1
rs890334
CNDP2
1.000 0.080 18 74521136 3 prime UTR variant A/G snv 0.95 1
rs846910
HSD11B1 ; HSD11B1-AS1
0.882 0.160 1 209701909 intron variant A/G snv 0.95 6
rs10466210
GRK5-IT1 ; GRK5
1.000 0.080 10 119210869 intron variant A/G snv 0.94 1
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 100
rs296766
LOC101927318 ; AQP2
1.000 0.080 12 49957170 3 prime UTR variant T/C snv 0.92 1
rs1423096 0.925 0.080 19 7674291 upstream gene variant T/C snv 0.92 2
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 26
rs10483032
CBR3-AS1 ; CBR3
1.000 0.080 21 36140267 intron variant A/G snv 0.90 1
rs2065929
LOC105378904 ; CHIAP3
1.000 0.080 1 111366982 intron variant G/A snv 0.89 1
rs316019
SLC22A2
0.790 0.360 6 160249250 missense variant A/C snv 0.90 0.89 8
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 24
rs2272592
DDAH2 ; CLIC1
1.000 0.080 6 31730575 5 prime UTR variant T/C snv 0.88 2
rs4740283 1.000 0.080 9 131572909 downstream gene variant G/A snv 0.87 1
rs10761745
JMJD1C
0.882 0.240 10 63341311 intron variant G/C snv 0.87 2
rs2970847
PPARGC1A
0.882 0.200 4 23814301 synonymous variant T/C snv 0.84 0.86 3
rs3731201
CDKN2A
1.000 0.080 9 21988897 intron variant C/T snv 0.86 2
rs13078
DICER1
0.827 0.280 14 95090410 3 prime UTR variant A/T snv 0.85 5
rs1887922
IDE
0.851 0.240 10 92464408 intron variant C/T snv 0.85 6
rs1884190
DLL1
1.000 0.080 6 170287611 intron variant C/T snv 0.85 1
rs2867125 0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85 2
rs1024610 0.882 0.200 17 34253212 upstream gene variant T/A snv 0.85 3
rs7100623
IDE
1.000 0.080 10 92567399 intron variant T/C snv 0.85 1
rs4930588 1.000 0.080 11 68647767 intergenic variant G/T snv 0.85 1