Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs764355898
NRK
1.000 0.080 X 105923145 missense variant A/C snv 7.9E-05 1.9E-05 1
rs368370244
PHKG1
1.000 0.080 7 56087718 missense variant C/T snv 3.6E-05 5.6E-05 1
rs764534677
PRKCB
1.000 0.080 16 24035448 missense variant G/A snv 8.0E-06 1
rs376894109
PRKCZ
1.000 0.080 1 2175293 missense variant C/T snv 4.0E-06 7.0E-06 1
rs781401034
PRKDC
1.000 0.080 8 47898527 missense variant C/T snv 1
rs149403911
RET
1.000 0.080 10 43102492 missense variant G/A;T snv 2.0E-05 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
rs774996232
RIPK1
1.000 0.080 6 3077805 missense variant C/T snv 1.6E-05 1.4E-05 1
rs140213020
ROR2
1.000 0.080 9 91724870 missense variant C/A;T snv 8.2E-06; 2.0E-05 1
rs376029388
RPS6KA2
1.000 0.080 6 166412769 missense variant C/T snv 1.3E-05 2.1E-05 1
rs539738963
STK40
1.000 0.080 1 36348807 missense variant C/T snv 2.2E-05 1.4E-05 1
rs755089893
STK40
1.000 0.080 1 36355378 missense variant A/G snv 4.0E-06; 8.0E-06 1
rs1262765773
TBK1
1.000 0.080 12 64485493 missense variant G/A snv 7.0E-06 1
rs1294404368
TRRAP
1.000 0.080 7 98981947 missense variant C/T snv 4.4E-06 1.4E-05 1
rs373632999
TRRAP
1.000 0.080 7 98949733 missense variant G/A snv 1.2E-05 4.2E-05 1
rs528967912
TRRAP
1.000 0.080 7 98964724 missense variant C/T snv 1.6E-05 7.0E-06 1
rs149061352
TTN
1.000 0.080 2 178785717 missense variant G/A;T snv 4.4E-05; 4.0E-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