Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34637584
LRRK2
0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs1805008
MC1R
0.732 0.240 16 89919736 missense variant C/T snv 4.7E-02 4.8E-02 16
rs356219
LOC105377329 ; SNCA
0.776 0.240 4 89716450 intron variant G/A snv 0.54 9
rs7133914
LRRK2
0.790 0.120 12 40309109 missense variant G/A;T snv 8.5E-02; 1.6E-05 7
rs7308720
LRRK2
0.790 0.120 12 40263898 missense variant C/A;G snv 4.0E-06; 8.7E-02 7
rs34311866
TMEM175
0.882 0.080 4 958159 missense variant T/C snv 0.18 0.14 6
rs12185268
MAPT-AS1 ; SPPL2C
0.851 0.160 17 45846317 missense variant A/G snv 0.15 0.14 5
rs1450426641
GBA
0.851 0.160 1 155235820 missense variant A/C snv 4.0E-06 4
rs11564148
LRRK2
0.851 0.080 12 40320099 missense variant T/A snv 0.30 0.27 4
rs894278
SNCA
0.882 0.080 4 89813384 intron variant T/G snv 0.15 4
rs6812193
FAM47E-STBD1 ; FAM47E ; LOC105377286
0.882 0.080 4 76277833 intron variant C/T snv 0.38 3
rs748055361
GAK
0.925 0.080 4 882749 missense variant A/G snv 4.0E-06 2
rs3756063
SNCA-AS1 ; SNCA
0.925 0.080 4 89836243 intron variant G/C snv 0.58 2
rs34884217
TMEM175
0.925 0.080 4 950422 splice acceptor variant A/C snv 7.0E-02 6.8E-02 2
rs11175964
LRRK2
1.000 0.080 12 40309185 synonymous variant G/A snv 7.5E-02 5.9E-02 1
rs1045722
SNCA
1.000 0.080 4 89724520 3 prime UTR variant T/A snv 0.24 1