Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10005233
SNCA
1.000 0.040 4 89822180 3 prime UTR variant C/T snv 0.58 0.59 1
rs10034259
LINC02503
1.000 0.040 4 104012596 intron variant A/C snv 0.19 1
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs10112596
GATA4
0.925 0.120 8 11722293 intron variant A/G snv 0.83 3
rs1017730
AGBL2
1.000 0.040 11 47711942 intron variant G/A snv 0.18 1
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs1049353
CNR1
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs10501320
MADD ; MADD-AS1
0.925 0.120 11 47272248 5 prime UTR variant G/C snv 0.17 5
rs10507274
C12orf49
1.000 0.040 12 116723171 missense variant T/C snv 4.7E-02 4.4E-02 2
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs1057518806
HMBS
1.000 0.040 11 119093155 frameshift variant G/- del 4
rs10769256
SPI1
1.000 0.040 11 47356845 intron variant C/G;T snv 1
rs10801153 0.925 0.080 1 192794818 intron variant G/A snv 0.27 3
rs10850379
MMAB
1.000 0.040 12 109564972 non coding transcript exon variant C/T snv 0.40 1
rs1085308045
PTEN
0.807 0.160 10 87933128 missense variant C/G;T snv 8
rs1085308056
PTEN
0.851 0.160 10 87957850 splice region variant C/G snv 8
rs10871777 0.925 0.120 18 60184530 intergenic variant A/G snv 0.24 6
rs110402
CRHR1 ; LINC02210-CRHR1 ; MAPT-AS1
0.790 0.120 17 45802681 intron variant G/A;C snv 12
rs11090045
ZC3H7B
1.000 0.040 22 41357599 3 prime UTR variant G/A;C snv 2
rs1110976
DRD2
1.000 0.040 11 113413797 intron variant T/G snv 3
rs11111
GDNF-AS1 ; GDNF
0.882 0.080 5 37814000 3 prime UTR variant T/C snv 0.22 5
rs11159097 1.000 0.040 14 74633180 intergenic variant T/A;C snv 1
rs11191392
WBP1L
1.000 0.040 10 102767194 intron variant C/A snv 0.49 1
rs11204421 1.000 0.040 17 19994492 intergenic variant T/C snv 0.44 1