Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057518011
TMEM240
1 1535766 missense variant C/T snv 4
rs2161961
GNAL
18 11774501 intron variant A/G snv 0.31 3
rs104895358
MVK
12 109595148 missense variant G/A snv 1.2E-05 2
rs121912703
ACE
17 63496977 missense variant C/T snv 3.7E-05 4.9E-05 2
rs12765063
CUL2 ; CREM
10 35127641 intron variant G/A snv 0.14 2
rs402691
PRKCG
19 53888383 intron variant T/C snv 0.39 2
rs1060504185
CDKN2A
9 21971116 missense variant G/A;C snv 1
rs1156401234
YARS2 ; DNM1L
12 32740421 missense variant G/A snv 4.0E-06 1
rs1334791875
APP
21 25982369 missense variant G/A snv 4.0E-06 1
rs1365502141
APP
21 26000017 missense variant G/A snv 7.0E-06 1
rs150450891
FTO
16 53826341 missense variant G/A snv 4.6E-04 5.7E-04 1
rs202064075
CLCNKB
1 16048352 missense variant G/A snv 1.5E-04 7.7E-05 1
rs539815495
PRKN
6 161973365 missense variant A/G snv 1.1E-04 1.4E-05 1
rs566794487
CRY1
12 106997986 missense variant A/C snv 3.6E-05 1
rs773857
CPAMD8
19 16908042 intron variant C/T snv 0.56 1
rs914655
C9orf92
9 16208133 intron variant G/T snv 1.6E-02 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93