Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs767181086
LAMC2
0.827 0.240 1 183220922 stop gained G/A;T snv 8.0E-06; 4.0E-06 11
rs74315405
PRNP
0.827 0.160 20 4699813 missense variant T/C snv 6
rs3865444
CD33
0.851 0.160 19 51224706 upstream gene variant C/A snv 0.25 8
rs744373 0.851 0.160 2 127137039 downstream gene variant A/G snv 0.35 8
rs393152
LINC02210 ; LINC02210-CRHR1
0.851 0.160 17 45641777 non coding transcript exon variant A/G snv 0.18 0.29 7
rs372805579
CARD14
0.851 0.200 17 80195302 missense variant G/A snv 2.4E-05 2.8E-05 5
rs610932
MS4A6A
0.851 0.080 11 60171834 downstream gene variant T/G snv 0.57 5
rs74315406
PRNP
0.851 0.160 20 4699870 missense variant A/G snv 5
rs74315412
PRNP
0.851 0.120 20 4699843 missense variant G/A snv 6.0E-05 3.5E-05 5
rs11538758
PRNP
0.882 0.160 20 4699534 missense variant C/A;T snv 8
rs74315402
PRNP
0.882 0.200 20 4699570 missense variant C/T snv 7
rs16990018
PRNP
0.882 0.120 20 4699732 missense variant A/G snv 3.8E-03 1.6E-02 5
rs74315414
PRNP
0.882 0.200 20 4699533 missense variant C/A;T snv 4.0E-06 5
rs11767557
EPHA1-AS1
0.882 0.080 7 143412046 intron variant T/C snv 0.18 4
rs193922906
PRNP
0.882 0.160 20 4699380 inframe insertion TCATGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCC/-;TCATGGTGGTGGCTGGGGGCAGCC;TCATGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCC;TCATGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCC delins 4
rs2736990
SNCA
0.882 0.080 4 89757390 intron variant G/A;T snv 4
rs2814707
LOC112268043 ; C9orf72 ; LOC107987057
0.882 0.120 9 27536399 non coding transcript exon variant C/G;T snv 4
rs74315411
PRNP
0.882 0.160 20 4699767 missense variant A/G snv 4
rs1178466848
PRNP
0.925 0.120 20 4699785 missense variant G/A snv 2.8E-05 4
rs398122370
PRNP
0.925 0.160 20 4699851 missense variant G/C snv 4
rs761807915
PRNP
0.925 0.120 20 4699824 missense variant G/A snv 4.0E-06 7.0E-06 4
rs1473972013
CYP4X1
0.925 0.160 1 47035911 missense variant G/A snv 7.0E-06 3
rs368821179
CARD14
0.925 0.160 17 80182758 missense variant T/C snv 8.0E-06 2.1E-05 3
rs398122414
PRNP
0.925 0.120 20 4699898 stop gained C/A snv 3
rs597668
BLOC1S3 ; MARK4
0.925 0.080 19 45205630 intron variant T/A;C;G snv 3