Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11552822
CDKN2A
1.000 9 21971109 missense variant C/A;T snv 4.3E-06 2
rs140926412
GDF3
0.925 12 7690177 missense variant G/A;T snv 2.0E-03; 4.0E-06 2
rs149925563
TTC21B ; TTC21B-AS1
0.925 2 165941046 missense variant T/A snv 1.1E-03 7.0E-04 2
rs1085307958
BRAT1
0.925 7 2544920 missense variant A/G snv 2
rs886039494
GNAO1
0.925 16 56336762 missense variant C/G;T snv 2
rs398122955
FAT4
0.925 4 125434349 missense variant G/A snv 4.0E-06 2
rs797045165
LZTR1
0.925 22 20991686 missense variant C/T snv 7.0E-06 2
rs776749939
SQSTM1
0.925 5 179833777 missense variant C/T snv 6.0E-05 1.4E-05 2
rs146013446
PPA2
0.925 4 105437964 missense variant C/T snv 4.9E-04 6.9E-04 2
rs587780076
TP53
17 7673743 missense variant C/A;T snv 8.0E-06; 8.0E-06 1
rs774057024
MRE11
11 94456331 missense variant C/T snv 1.6E-05 2.8E-05 1
rs748434421
MRE11
11 94485928 missense variant T/A snv 4.0E-06 1.4E-05 1
rs200085146
MRE11
11 94447287 missense variant C/T snv 2.0E-05 7.0E-06 1
rs869312784
APC
5 112838674 missense variant A/G snv 1
rs747621669
CDKN2A
9 21970988 missense variant C/T snv 4.1E-06 1
rs121913381
CDKN2A
9 21971037 missense variant C/A;T snv 1
rs137853213
COL9A2
1 40307477 missense variant TG/CA mnv 1
rs587777600
RAVER1 ; FDX2
19 10315996 missense variant T/A;G snv 1
rs888630930
ZGLP1 ; FDX2
19 10310616 missense variant G/A snv 1
rs121434328
HAL
12 95992772 missense variant C/A;T snv 3.6E-05 1
rs121434329
HAL
12 95990472 missense variant G/A snv 2.8E-05 2.1E-05 1
rs121434327
HAL
12 95992778 missense variant C/G;T snv 1.2E-05; 3.2E-05 1
rs121434330
HAL
12 95987153 missense variant C/G;T snv 2.0E-05 1
rs28941786
CTH
1 70430388 stop gained C/G;T snv 8.0E-06; 4.0E-06 1
rs116840786
CAV3 ; SSUH2
3 8733962 missense variant C/A;T snv 1