Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1337040042
AATK
1.000 0.040 17 81131085 start lost T/C snv 1
rs773301216
CDK14
1.000 0.040 7 91118066 missense variant G/A snv 4.0E-06 1.4E-05 1
rs755711267
CDKL2
1.000 0.040 4 75607279 missense variant C/T snv 3.6E-05 2.8E-05 1
rs1057519893
ERBB3
0.790 0.160 12 56085070 missense variant G/A;T snv 1
rs753734841
KRTCAP3 ; NRBP1
1.000 0.040 2 27440906 missense variant C/T snv 1.2E-05 1.4E-05 1
rs375029799
LOC101927055 ; TTN-AS1 ; TTN
1.000 0.040 2 178776873 missense variant C/T snv 2.4E-05 2.1E-05 1
rs200212150
LRRK2
1.000 0.040 12 40314084 missense variant G/A;T snv 1.6E-05 1.4E-05 1
rs144052967
MELK
1.000 0.040 9 36665552 missense variant C/T snv 1.3E-04 6.3E-05 1
rs1423134583
MYO3A
1.000 0.040 10 26096393 missense variant T/A snv 4.0E-06 1
rs201821707
NEK10
1.000 0.040 3 27346152 missense variant G/A;C;T snv 3.4E-04; 6.0E-05; 4.0E-06 1
rs374535834
RPS6KB2 ; CORO1B ; PTPRCAP ; RPS6KB2-AS1
1.000 0.040 11 67435048 missense variant C/A;T snv 4.1E-06; 6.5E-05 1
rs746238409
RYK
1.000 0.040 3 134202791 missense variant C/T snv 2.8E-05 2.1E-05 1
rs368877591
SNRK-AS1 ; SNRK
1.000 0.040 3 43348090 missense variant G/A snv 5.9E-05 1.4E-05 1
rs762000831
SPEG ; ASIC4-AS1
1.000 0.040 2 219483170 missense variant C/T snv 8.9E-05 1.4E-05 1
rs113498671
TNK2
1.000 0.040 3 195884972 missense variant C/T snv 8.0E-06 1
rs370624303
ULK1
1.000 0.040 12 131910720 missense variant G/A snv 3.2E-05 2.1E-05 1
rs200610853
WEE2 ; WEE2-AS1
1.000 0.040 7 141724247 missense variant G/A snv 4.0E-06 7.0E-06 1