Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs539738963
STK40
1.000 0.080 1 36348807 missense variant C/T snv 2.2E-05 1.4E-05 1
rs555460132
CAMK2B
1.000 0.080 7 44228798 missense variant G/A snv 1.9E-04 2.0E-04 1
rs587779858
ATM
1.000 0.080 11 108227692 missense variant G/A snv 1
rs587782310
C11orf65 ; ATM
1.000 0.080 11 108330234 missense variant G/A snv 8.0E-06 7.0E-06 1
rs730881315
ATM ; C11orf65
1.000 0.080 11 108329154 stop gained C/A;T snv 4.0E-06; 8.0E-06 1
rs751005114
KIT
1.000 0.080 4 54731395 missense variant G/A snv 8.0E-06 7.0E-06 1
rs751398376
TTN ; TTN-AS1
1.000 0.080 2 178609836 missense variant C/A;G snv 1.2E-05; 4.0E-06 1
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