Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs753665559
MAP2K4
1.000 0.080 17 12125315 missense variant G/A snv 4.0E-06 1
rs755089893
STK40
1.000 0.080 1 36355378 missense variant A/G snv 4.0E-06; 8.0E-06 1
rs758268804
RIPK1
1.000 0.080 6 3077855 missense variant G/A snv 3.2E-05 1.0E-04 1
rs759012409
RIPK1
1.000 0.080 6 3083284 missense variant C/T snv 4.1E-06 7.0E-06 1
rs764355898
NRK
1.000 0.080 X 105923145 missense variant A/C snv 7.9E-05 1.9E-05 1
rs764534677
PRKCB
1.000 0.080 16 24035448 missense variant G/A snv 8.0E-06 1
rs765563230
LOC339874 ; NEK11
1.000 0.080 3 131349687 missense variant G/A snv 2.0E-05 3.5E-05 1
rs774996232
RIPK1
1.000 0.080 6 3077805 missense variant C/T snv 1.6E-05 1.4E-05 1
rs778726488
MATK
1.000 0.080 19 3778199 missense variant C/G;T snv 1.7E-05 1
rs780763668
MARK4
1.000 0.080 19 45280710 missense variant C/A;T snv 4.0E-06; 8.0E-06 1
rs781401034
PRKDC
1.000 0.080 8 47898527 missense variant C/T snv 1
rs952665081
LOC105372523 ; PAK5
1.000 0.080 20 9580201 missense variant A/G snv 1
rs137853200
EPHA2
0.925 0.120 1 16129440 missense variant G/A snv 1
rs137853007
CHEK2
0.790 0.240 22 28725254 missense variant G/A;T snv 5.2E-05 2
rs202160435
ATM
0.925 0.240 11 108247072 missense variant G/A snv 8.0E-05 6.3E-05 1
rs121913361
BRAF
0.807 0.280 7 140753349 missense variant C/A;G;T snv 1
rs121913370
BRAF
0.763 0.360 7 140753393 missense variant T/C;G snv 1
rs121913355
BRAF
0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 4
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 1