Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2306604
TFAM
0.827 0.080 10 58388932 intron variant A/C;G;T snv 5
rs377591051
PRKN
0.851 0.080 6 162262651 missense variant C/T snv 4.0E-06 7.0E-06 4
rs104893936
SNCB
0.851 0.120 5 176626472 missense variant C/G;T snv 5.6E-05 4
rs104893937
SNCB
0.851 0.120 5 176621218 missense variant G/T snv 1.7E-04 2.0E-04 4
rs113388242
EIF4G1
0.925 0.080 3 184327376 missense variant C/T snv 4.0E-05 7.0E-05 3
rs774457232
EIF4G1
0.925 0.080 3 184331303 missense variant G/A;T snv 6.4E-05 3
rs35749011 0.925 0.080 1 155162560 intergenic variant G/A snv 1.1E-02 2
rs616338
ABI3
0.925 0.080 17 49219935 missense variant T/C snv 0.99 0.99 2
rs1041833271
APP
0.925 0.080 21 25975995 missense variant C/T snv 7.0E-06 2
rs12734374
ASH1L
1.000 0.080 1 155419060 intron variant A/T snv 3.4E-02 2
rs897984
MIR762HG ; BCL7C ; MIR4519
0.925 0.080 16 30875322 non coding transcript exon variant T/C snv 0.62 0.47 2
rs1446915570
PSEN1
0.925 0.080 14 73173623 synonymous variant A/T snv 4.0E-06 7.0E-06 2
rs777296100
SNCA
0.925 0.080 4 89725318 3 prime UTR variant -/TAA;TAAAA ins 2
rs1330229174
SNCA ; SNCA-AS1
0.925 0.080 4 89835568 missense variant T/C snv 4.0E-06 2
rs1342971994
SNCA
1.000 0.080 4 89822344 missense variant C/T snv 1.4E-05 1
rs7681440
SNCA-AS1 ; SNCA
1.000 0.080 4 89835399 intron variant C/A;G snv 1