Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs28933979
TTR
0.587 0.600 18 31592974 missense variant G/A;C snv 1.0E-04 70
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs75932628
LOC105375056 ; TREM2
0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
rs1805007
MC1R
0.695 0.280 16 89919709 missense variant C/A;G;T snv 4.4E-02 25
rs10719
DROSHA
0.677 0.680 5 31401340 3 prime UTR variant A/G;T snv 0.69 24
rs104893878
SNCA ; SNCA-AS1
0.732 0.160 4 89835580 missense variant C/G snv 21
rs4746
GLO1
0.708 0.400 6 38682852 missense variant T/A;G snv 0.36 21
rs4918
AHSG
0.763 0.400 3 186620593 missense variant G/A;C snv 0.67 12
rs7895833 0.742 0.440 10 67863299 upstream gene variant G/A;C snv 12
rs3736265
PPARGC1A
0.790 0.360 4 23813084 missense variant G/A;T snv 8.6E-02; 2.8E-05 7
rs62643364
PRNP
0.851 0.160 20 4699466 synonymous variant A/G;T snv 4.0E-06; 1.4E-04 7
rs121917767
UCHL1
0.827 0.120 4 41260751 missense variant C/A;G;T snv 4.0E-05; 4.0E-06; 2.0E-05 6
rs9657182
IDO1
0.851 0.280 8 39908329 intron variant C/G;T snv 6
rs200161705
NEK1
0.882 0.160 4 169585374 missense variant C/A;T snv 6.0E-05; 2.3E-03 5
rs2281997
ENHO
0.882 0.240 9 34521869 intron variant T/A;C snv 5
rs2292779
AGO2
0.851 0.320 8 140551294 intron variant G/C;T snv 0.57; 4.9E-06 4
rs150393409
FAN1
0.882 0.200 15 30910758 missense variant G/A;C snv 6.6E-03; 6.0E-05 3
rs2742976
E2F2
0.882 0.240 1 23531510 upstream gene variant T/A;G snv 3