Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 3
rs281865127
MPZ
0.827 0.120 1 161306767 missense variant T/C snv 3
rs34993780
UGT1A10 ; MROH2A ; UGT1A7 ; UGT1A5 ; UGT1A6 ; UGT1A1 ; UGT1A9 ; UGT1A8 ; UGT1A3 ; UGT1A4
0.827 0.120 2 233772413 missense variant T/A;C;G snv 2.2E-04 3
rs121913274
PIK3CA
0.645 0.320 3 179218304 missense variant A/C;G;T snv 3
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 3
rs75996173
RET
0.716 0.240 10 43114501 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 3
rs77939446
RET
0.724 0.120 10 43113622 missense variant G/A;C;T snv 4.0E-06 3
rs79781594
RET
0.732 0.160 10 43113649 missense variant G/A;C;T snv 3
rs77709286
RET
0.752 0.160 10 43114502 missense variant C/G snv 4.0E-06 3
rs76262710
RET
0.724 0.280 10 43113648 missense variant T/A;C;G snv 4.0E-06; 4.0E-06 3
rs75076352
RET
0.689 0.240 10 43114500 missense variant T/A;C;G snv 1.2E-05 3
rs121913322
STK11
0.882 0.120 19 1221320 missense variant C/A;G;T snv 2.9E-05; 1.2E-04 3
rs137852564
AR
0.827 0.240 X 67722976 missense variant G/A;T snv 3
rs121913413
CTNNB1
0.763 0.240 3 41224634 missense variant C/A;T snv 3
rs121913403
CTNNB1
0.683 0.240 3 41224622 missense variant C/A;G;T snv 3
rs776587763
FGFR2
0.790 0.120 10 121520085 missense variant C/A;T snv 4.0E-06; 4.0E-06 3
rs121918502
FGFR2
0.790 0.160 10 121517351 missense variant G/C snv 3
rs80338958
SCN4A
0.790 0.200 17 63945614 missense variant C/A;T snv 1.6E-05; 5.6E-05 3
rs192732174
GLB1
0.827 0.160 3 33068245 missense variant G/A;T snv 4.0E-05; 3.6E-05 3
rs137853006
PROM1
0.776 0.080 4 16013299 missense variant G/A snv 3
rs28940291
MFN2
0.776 0.080 1 11992660 missense variant G/A snv 4.0E-06 3
rs57520892
LMNA
0.776 0.200 1 156137204 missense variant G/A;C snv 4.1E-05 3
rs121908670
LRP5
0.882 0.080 11 68363784 missense variant G/A snv 3
rs80359818
SLC2A1
0.776 0.360 1 42930766 missense variant G/A snv 3
rs201893408
TMEM67
0.695 0.480 8 93795970 missense variant T/A;C snv 8.0E-06; 1.5E-04 3