Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2236225
MTHFD1
0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 52
rs16969968
CHRNA5
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 37
rs1386984902
APP
0.790 0.160 21 26000095 missense variant G/A snv 9
rs1018381
DTNBP1
0.882 0.040 6 15656839 intron variant G/A snv 0.16 6
rs6584400
NRG3
0.851 0.120 10 81896770 intron variant G/A snv 0.22 6
rs75548401
GBA
0.882 0.160 1 155236246 missense variant G/A snv 5.9E-03 6.2E-03 6
rs8074995
PRKCA
0.925 0.040 17 66796013 intron variant G/A snv 0.13 5
rs1800557
APP
0.925 0.040 21 25891795 missense variant G/A snv 4.0E-05 4.2E-05 3
rs1329650
HECTD2-AS1
0.882 0.080 10 91588363 regulatory region variant G/A;T snv 6
rs761715536
ADRA2A
1.000 0.040 10 111079092 stop gained G/A;T snv 6.4E-06; 1.3E-05 3
rs63750082
PSEN1
0.732 0.120 14 73192712 missense variant G/C;T snv 8.0E-06 13
rs77369218
GBA
0.807 0.160 1 155235726 missense variant T/A snv 7
rs2189814
GRM3
0.925 0.040 7 86702440 intron variant T/A;C snv 3
rs572842823
APP
0.763 0.160 21 25897626 missense variant T/A;G snv 11
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs1611115
DBH
0.732 0.280 9 133635393 upstream gene variant T/C snv 0.80 16
rs10748842
NRG3
0.807 0.120 10 81889983 intron variant T/C snv 0.13 8
rs1245342105
SPTBN1
1.000 0.040 2 54622367 missense variant T/C snv 4.0E-06 2
rs1051266
SLC19A1
0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs63750756
MAPT
0.716 0.200 17 46010324 missense variant T/G snv 2.6E-05 23