Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11248051
GAK
1.000 0.040 4 864544 intron variant C/G;T snv 1
rs11931074
SNCA ; LOC105377329
0.851 0.080 4 89718364 intron variant G/A;C;T snv 1
rs12726330
SLC50A1
1.000 0.040 1 155135691 splice region variant G/A;C snv 1.1E-02; 3.4E-05 1
rs1468375 1.000 0.040 7 145337519 intergenic variant C/A;T snv 1
rs181489
LOC105377329 ; SNCA
1.000 0.040 4 89713869 intron variant T/A;C snv 1
rs199498
WNT3 ; LRRC37A2
0.925 0.120 17 46788237 intron variant T/C;G snv 1
rs2066842
NOD2
0.763 0.200 16 50710713 missense variant C/A;T snv 4.0E-06; 0.19 1
rs2298728
SNCA
1.000 0.040 4 89821664 intron variant G/A;T snv 1
rs2338971 1.000 0.040 1 101414449 intergenic variant T/A;C snv 1
rs2583988
SNCA-AS1 ; SNCA
0.925 0.080 4 89839677 non coding transcript exon variant C/A;T snv 1
rs356220
LOC105377329 ; SNCA
0.925 0.080 4 89720189 intron variant T/A;C snv 1
rs356229
LOC105377329
1.000 0.040 4 89685446 non coding transcript exon variant C/A;T snv 1
rs3857059
SNCA
1.000 0.040 4 89754087 intron variant A/G;T snv 1
rs4130047
RIT2
0.925 0.080 18 43098270 intron variant T/A;C snv 1
rs4698412
BST1
1.000 0.040 4 15735725 intron variant G/A;T snv 1
rs6532194 1.000 0.040 4 89859751 intergenic variant C/G;T snv 1
rs6599389
TMEM175
1.000 0.040 4 945325 intron variant G/A;T snv 1
rs6656401
CR1
0.776 0.200 1 207518704 intron variant A/G;T snv 1
rs6757197 1.000 0.040 2 158866994 intron variant G/C;T snv 1
rs7304279
LOC112268095 ; SLC2A13
1.000 0.040 12 40072140 intron variant T/A;C snv 1
rs7521
MAPT ; KANSL1
0.925 0.080 17 46028029 3 prime UTR variant A/C;G snv 1
rs75932628
LOC105375056 ; TREM2
0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 1
rs7655536
LOC105377286 ; FAM47E-STBD1 ; FAM47E
1.000 0.040 4 76255615 intron variant T/A;C snv 1
rs7666265
FAM47E-STBD1 ; LOC105377286 ; FAM47E
1.000 0.040 4 76255128 intron variant G/A;T snv 1
rs870575
LINC01121
1.000 0.040 2 45276121 intron variant G/A;C snv 1