Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1474322770
NKX2-1 ; NKX2-1-AS1 ; SFTA3
0.827 0.240 14 36519251 missense variant G/A snv 5
rs2124459
CBS
0.827 0.200 21 43055604 3 prime UTR variant T/C snv 0.36 5
rs2239907
SARM1 ; SLC46A1
0.851 0.200 17 28398728 3 prime UTR variant T/C snv 0.53 5
rs2326398
CRISPLD2
0.827 0.200 16 84869111 intron variant A/G snv 0.37 5
rs3771523
TGFA
0.851 0.200 2 70450336 3 prime UTR variant C/T snv 0.14 5
rs493760
DROSHA
0.851 0.200 5 31436933 intron variant C/T snv 0.74 5
rs560426
ABCA4
0.851 0.200 1 94087882 intron variant C/T snv 0.53 5
rs739439
SLC46A1 ; SARM1
0.851 0.200 17 28396803 3 prime UTR variant C/T snv 0.13 5
rs786205508
MKS1
0.851 0.200 17 58208542 stop gained G/A snv 5
rs1139
ZNF385B
0.851 0.200 2 179745354 intron variant C/T snv 0.22 4
rs1553547838
SATB2
0.925 0.280 2 199328709 stop gained G/A snv 4
rs197204
MCUB
0.851 0.200 4 109576918 intron variant C/G snv 0.52 4
rs28937575
FOXE1 ; PTCSC2
0.851 0.280 9 97854084 missense variant G/A snv 4
rs6757845
ZNF385B
0.851 0.200 2 179449268 intron variant T/C snv 0.66 4
rs8179096
TIMP2
0.851 0.200 17 78925567 upstream gene variant G/A;C snv 4
rs1057519583
STN1
0.882 0.160 10 103900115 missense variant C/G snv 3
rs11624283 0.882 0.200 14 105124634 downstream gene variant A/G snv 0.13 3
rs2237138
JARID2
0.882 0.200 6 15463164 intron variant T/C snv 0.22 3
rs227493 0.882 0.200 6 165071698 intron variant A/T snv 1.7E-02 3
rs3905385
ROR2
0.882 0.200 9 91906451 intron variant T/C snv 0.23 3
rs7205289
WWP2 ; MIR140
0.882 0.200 16 69933102 non coding transcript exon variant C/A snv 3
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs765462548
STN1
0.882 0.160 10 103898989 missense variant C/A;T snv 4.0E-06; 2.4E-05 3
rs79184941
FGFR2
0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 41
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193