Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10015979
HTT
1.000 0.120 4 3107715 intron variant A/G snv 0.30 1
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs104893878
SNCA ; SNCA-AS1
0.732 0.160 4 89835580 missense variant C/G snv 21
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1057035
DICER1
0.763 0.440 14 95087805 3 prime UTR variant T/C snv 0.26 12
rs10719
DROSHA
0.677 0.680 5 31401340 3 prime UTR variant A/G;T snv 0.69 24
rs10881578
RXRA
0.925 0.240 9 134340689 intron variant A/G snv 0.32 2
rs10934657
KALRN
1.000 0.120 3 124093989 intron variant T/C snv 0.60 1
rs10937921 1.000 0.120 4 3274764 downstream gene variant C/T snv 0.40 2
rs11039155
NR1H3
0.827 0.400 11 47259211 5 prime UTR variant G/A snv 0.14 0.12 6
rs110501
HTT
1.000 0.120 4 3223751 intron variant T/C snv 0.47 1
rs11248108
RNF4
1.000 0.120 4 2479763 intron variant G/A;T snv 1
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1138690 1.000 0.120 4 3289674 upstream gene variant G/A;T snv 1
rs1170668763
BECN1
1.000 0.120 17 42818395 missense variant T/A snv 7.0E-06 1
rs11731237
HTT
1.000 0.120 4 3150086 intron variant C/T snv 0.26 1
rs1210554604
HTT
1.000 0.120 4 3131662 missense variant G/A snv 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121917767
UCHL1
0.827 0.120 4 41260751 missense variant C/A;G;T snv 4.0E-05; 4.0E-06; 2.0E-05 6
rs1232027
LINC01337
1.000 0.120 5 80619201 intron variant G/A snv 0.32 1
rs12641989
RGS12
1.000 0.120 4 3418113 non coding transcript exon variant G/A;C snv 1
rs12668183 1.000 0.120 7 16455781 regulatory region variant T/C snv 0.34 1
rs1272951905
MTHFSD
0.925 0.160 16 86532210 missense variant C/T snv 2.1E-05 3