Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 58
rs104893878
SNCA ; SNCA-AS1
0.732 0.160 4 89835580 missense variant C/G snv 20
rs104893875
SNCA
0.742 0.120 4 89828170 missense variant C/T snv 4.0E-06 12
rs356219
LOC105377329 ; SNCA
0.776 0.240 4 89716450 intron variant G/A snv 0.54 9
rs431905511
SNCA
0.827 0.080 4 89828154 missense variant C/T snv 8
rs11931074
SNCA ; LOC105377329
0.851 0.080 4 89718364 intron variant G/A;C;T snv 7
rs542171324
SNCA
0.851 0.160 4 89828148 missense variant G/A;C snv 8.0E-06; 4.0E-06 6
rs201106962
SNCA
0.851 0.080 4 89828156 missense variant A/C snv 8.0E-05 7.0E-05 4
rs17016074
SNCA
0.851 0.080 4 89726127 3 prime UTR variant G/A snv 4.7E-02 4
rs894278
SNCA
0.882 0.080 4 89813384 intron variant T/G snv 0.15 4
rs356182
LOC105377329 ; SNCA
0.882 0.080 4 89704960 intron variant G/A snv 0.65 3
rs356220
LOC105377329 ; SNCA
0.925 0.080 4 89720189 intron variant T/A;C snv 3
rs356200
SNCA
0.882 0.160 4 89747463 intron variant T/C snv 0.44 3
rs356165
SNCA
0.882 0.080 4 89725735 3 prime UTR variant G/A snv 0.54 3
rs2736990
SNCA
0.882 0.080 4 89757390 intron variant G/A;T snv 3
rs3857059
SNCA
1.000 0.040 4 89754087 intron variant A/G;T snv 2
rs777296100
SNCA
0.925 0.080 4 89725318 3 prime UTR variant -/TAA;TAAAA ins 2
rs2583988
SNCA-AS1 ; SNCA
0.925 0.080 4 89839677 non coding transcript exon variant C/A;T snv 2
rs3756063
SNCA-AS1 ; SNCA
0.925 0.080 4 89836243 intron variant G/C snv 0.58 2
rs1330229174
SNCA ; SNCA-AS1
0.925 0.080 4 89835568 missense variant T/C snv 4.0E-06 2
rs356221
LOC105377329 ; SNCA
1.000 0.040 4 89721313 intron variant A/T snv 0.44 1
rs356181
LOC105377329 ; SNCA
1.000 0.040 4 89704988 intron variant G/A snv 0.46 1
rs181489
LOC105377329 ; SNCA
1.000 0.040 4 89713869 intron variant T/A;C snv 1
rs10516846
SNCA
1.000 0.080 4 89775184 intron variant A/G snv 3.9E-02 1
rs356168
SNCA
1.000 0.040 4 89753280 intron variant G/A snv 0.45 1