Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057518988
GRIN2B
0.925 0.040 12 13571859 missense variant T/C snv 3
rs58982919
NEFL
0.790 0.080 8 24956223 missense variant T/C snv 3
rs74315402
PRNP
0.882 0.200 20 4699570 missense variant C/T snv 3
rs120074125
SMPD1
0.882 0.160 11 6393301 missense variant T/G snv 4.0E-06 3
rs121908225
CACNA1A
0.790 0.120 19 13365448 missense variant G/A snv 2
rs755221106
CACNA1G
0.851 0.040 17 50617560 missense variant G/A;T snv 4.0E-06 2
rs876661219
GRIN2B
1.000 12 13571891 missense variant A/C;G snv 2
rs28933383
KCNA1
0.851 0.120 12 4912055 missense variant C/A;G;T snv 2
rs886041761
KCNA2
0.925 0.200 1 110603902 missense variant C/T snv 2
rs143319805
OPA1
0.807 0.320 3 193643378 missense variant A/G snv 6.2E-04 5.7E-04 2
rs11538758
PRNP
0.882 0.160 20 4699534 missense variant C/A;T snv 2
rs74315401
PRNP
0.683 0.320 20 4699525 missense variant C/T snv 2
rs121918544
TINF2
0.827 0.200 14 24240635 missense variant C/T snv 2
rs201754030
TSFM
0.925 0.200 12 57796461 stop gained C/T snv 1.5E-03 1.3E-03 2
rs121918100
TTR
0.827 0.160 18 31595184 missense variant T/C snv 2
rs267606695
CA8
1.000 0.160 8 60266044 missense variant A/C;G snv 1
rs121908230
CACNA1A
0.882 0.080 19 13262789 missense variant C/T snv 1
rs771578775
COQ8A
1.000 0.080 1 226982996 stop gained C/T snv 4.5E-05 5.6E-05 1
rs104894107
FXN
0.882 0.160 9 69064942 missense variant G/C;T snv 3.6E-05; 2.8E-05 1
rs118204095
HMBS
1.000 0.160 11 119091414 missense variant G/A;T snv 4.5E-05 1
rs118204096
HMBS
1.000 0.160 11 119091432 missense variant G/A snv 1
rs587777004
HNRNPU ; COX20
1.000 0.080 1 244842055 missense variant A/C;G snv 4.0E-06 1
rs28933381
KCNA1
0.925 0.080 12 4912102 missense variant G/C snv 1
rs104894699
KCNC3
0.925 0.120 19 50323694 missense variant C/T snv 1
rs137852763
MRE11
0.851 0.320 11 94476318 missense variant C/G snv 1