Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs429699
SLC6A3
0.925 0.080 5 1409012 intron variant T/C snv 0.96 0.98 3
rs1384236
SLC2A13
1.000 0.040 12 40064582 intron variant C/T snv 0.95 1
rs4768212
LOC112268095 ; SLC2A13
1.000 0.040 12 40080345 intron variant C/T snv 0.95 1
rs370
EEF1DP3 ; FRY
1.000 0.040 13 31908207 intron variant T/C snv 0.93 1
rs2451078
TPTE2
1.000 0.040 13 19524149 intron variant G/C snv 0.93 1
rs10737170
LMNA
1.000 0.040 1 156094089 intron variant C/A snv 0.90 1
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 24
rs6746030
SCN1A-AS1 ; SCN9A
0.763 0.320 2 166242648 missense variant A/G snv 0.88 0.88 16
rs823128
NUCKS1
1.000 0.040 1 205744250 intron variant G/A snv 0.88 1
rs10247962
TFR2
1.000 0.040 7 100622306 intron variant G/A snv 0.88 2
rs2744687
PRDM2
1.000 0.040 1 13812318 intron variant T/G snv 0.88 1
rs2744690
PRDM2
1.000 0.040 1 13811306 intron variant A/C snv 0.87 1
rs2421095
SPR
1.000 0.040 2 72886395 upstream gene variant G/A snv 0.86 1
rs415430
WNT3 ; LRRC37A2
1.000 0.040 17 46781778 intron variant C/T snv 0.84 3
rs199515
WNT3 ; LRRC37A2
0.925 0.120 17 46779275 intron variant G/C snv 0.84 3
rs823122 1.000 0.040 1 205755900 intergenic variant C/T snv 0.83 1
rs3785883
MAPT
0.925 0.080 17 45977067 non coding transcript exon variant A/G snv 0.81 2
rs168552
LOC105377329 ; SNCA
1.000 0.040 4 89721993 intron variant C/T snv 0.80 1
rs356186
SNCA
1.000 0.040 4 89784213 intron variant A/G snv 0.80 1
rs1611115
DBH
0.732 0.280 9 133635393 upstream gene variant T/C snv 0.80 16
rs35479735
NR4A2
1.000 0.040 2 156326700 intron variant C/- delins 0.71 0.79 1
rs1051931
PLA2G7
0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs2197120
SNCA
1.000 0.040 4 89808451 intron variant A/G snv 0.78 1
rs1372520
SNCA ; SNCA-AS1
1.000 0.040 4 89836354 intron variant T/C snv 0.78 1
rs356180
SNCA ; LOC105377329
1.000 0.040 4 89706976 intron variant A/G snv 0.77 1