Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs745410279
IGF1
0.925 0.200 12 102478498 missense variant T/C snv 4.1E-06 2
rs267607048
SHOC2
0.752 0.560 10 110964362 missense variant A/G snv 7.0E-06 16
rs267606990
RPL6 ; PTPN11
0.851 0.240 12 112419116 missense variant C/T snv 4
rs397507501
PTPN11
0.882 0.160 12 112446385 missense variant A/G snv 5
rs397507503
PTPN11
1.000 0.160 12 112450335 missense variant C/T snv 1
rs397507504
PTPN11
0.925 0.160 12 112450346 missense variant A/G snv 7.0E-06 2
rs397507505
PTPN11
0.827 0.240 12 112450352 missense variant A/C;G;T snv 5
rs397507506
PTPN11
0.807 0.240 12 112450354 missense variant C/A;G snv 6
rs397507507
PTPN11
1.000 0.160 12 112450358 missense variant G/A;C;T snv 1
rs397507509
PTPN11
0.807 0.240 12 112450359 missense variant G/C;T snv 9
rs397507510
PTPN11
0.776 0.280 12 112450361 missense variant G/A;C;T snv 8
rs121918461
PTPN11
0.827 0.240 12 112450362 missense variant A/C;G;T snv 12
rs121918460
PTPN11
0.708 0.400 12 112450364 missense variant T/A;G snv 4.0E-06 27
rs121918459
PTPN11
0.662 0.440 12 112450368 missense variant A/G snv 1.2E-05 7.0E-06 47
rs1057517917
PTPN11
0.925 0.200 12 112450368 missense variant AT/GC mnv 2
rs397507511
PTPN11
0.882 0.240 12 112450385 missense variant G/A;C snv 3
rs727503380
PTPN11
0.925 0.160 12 112450386 missense variant A/T snv 2
rs397516801
PTPN11
0.925 0.160 12 112450389 missense variant A/G snv 2
rs397507512
PTPN11
0.925 0.160 12 112450391 missense variant T/C;G snv 2
rs121918453
PTPN11
0.732 0.280 12 112450394 missense variant G/A;C;T snv 19
rs121918454
PTPN11
0.742 0.280 12 112450395 missense variant C/A;G;T snv 17
rs397516802
PTPN11
1.000 0.160 12 112450397 missense variant AC/CT mnv 1
rs121918462
PTPN11
0.742 0.320 12 112450398 missense variant C/T snv 13
rs121918464
PTPN11
0.708 0.440 12 112450406 missense variant G/A;C snv 25
rs397507514
PTPN11
0.790 0.240 12 112450408 missense variant G/C;T snv 10