Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10165970
NPAS2
0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs17024869
NPAS2
0.708 0.320 2 100843581 intron variant T/C snv 8.3E-02 18
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35 23
rs7581886
NPAS2
0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs6214
LINC02456 ; HELLPAR ; IGF1
0.672 0.400 12 102399791 3 prime UTR variant C/T snv 0.45 26
rs2195239
LINC02456 ; IGF1
0.851 0.240 12 102462924 non coding transcript exon variant C/G snv 0.28 7
rs2162679
IGF1
0.851 0.240 12 102477481 intron variant C/G;T snv 6
rs2001389
SUFU
0.925 0.120 10 102615501 intron variant G/A;C snv 3
rs2094258
ERCC5 ; BIVM-ERCC5
0.701 0.280 13 102844409 intron variant C/T snv 0.18 20
rs7859034
SMC2
0.851 0.120 9 104103411 intron variant G/T snv 0.60 4
rs2417487
SMC2
1.000 0.120 9 104125300 intron variant A/G;T snv 1
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs1273593548
PIK3CG
0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19
rs1412335442
PIK3CG
0.925 0.120 7 106868317 missense variant G/T snv 7.0E-06 2
rs4988483
SSTR5-AS1 ; SSTR5
0.752 0.240 16 1079010 missense variant C/A snv 3.7E-02 3.7E-02 11
rs4988487
SSTR5 ; SSTR5-AS1
0.925 0.120 16 1079193 missense variant C/A;T snv 4.0E-06; 5.3E-02 2
rs169068
SSTR5-AS1 ; SSTR5
0.742 0.280 16 1079872 missense variant C/T snv 0.54 0.50 12
rs786203926
ATM
0.882 0.120 11 108227678 synonymous variant T/C snv 4
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 39
rs200027650
TCHP
1.000 0.120 12 109904025 missense variant G/A snv 2.5E-04 1.4E-04 1
rs11085754
SMARCA4
0.925 0.120 19 11017920 intron variant A/G snv 0.41 2
rs940553638
ALDH2
0.827 0.200 12 111783222 missense variant G/A snv 1.6E-05 7.0E-06 6
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs351365
WNT2B
1.000 0.120 1 112503773 intron variant T/C;G snv 1
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93