Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs914655
C9orf92
9 16208133 intron variant G/T snv 1.6E-02 1
rs1060504185
CDKN2A
9 21971116 missense variant G/A;C snv 1
rs202064075
CLCNKB
1 16048352 missense variant G/A snv 1.5E-04 7.7E-05 1
rs773857
CPAMD8
19 16908042 intron variant C/T snv 0.56 1
rs566794487
CRY1
12 106997986 missense variant A/C snv 3.6E-05 1
rs150450891
FTO
16 53826341 missense variant G/A snv 4.6E-04 5.7E-04 1
rs539815495
PRKN
6 161973365 missense variant A/G snv 1.1E-04 1.4E-05 1
rs1156401234
YARS2 ; DNM1L
12 32740421 missense variant G/A snv 4.0E-06 1
rs121912703
ACE
17 63496977 missense variant C/T snv 3.7E-05 4.9E-05 2
rs776423109
C3
1.000 0.120 19 6718117 missense variant G/A;T snv 4.0E-06; 4.0E-06 2
rs1331851285
CASP1
1.000 0.080 11 105029220 missense variant T/C snv 1.4E-05 2
rs12765063
CUL2 ; CREM
10 35127641 intron variant G/A snv 0.14 2
rs6278
DRD2
1.000 0.080 11 113410002 3 prime UTR variant C/A snv 0.14 2
rs1057519475
FOXC1
1.000 0.080 6 1610761 stop gained C/T snv 2
rs372857241
FOXC1
1.000 0.080 6 1610586 stop gained C/G;T snv 1.8E-05 2
rs1541665
KCNIP1
1.000 0.040 5 170715913 intron variant C/G;T snv 0.21 2
rs202247812
KRAS
1.000 0.160 12 25225717 missense variant T/C snv 2
rs942758928
MC4R
1.000 0.080 18 60371854 missense variant C/T snv 8.0E-06 1.4E-05 2
rs104895358
MVK
12 109595148 missense variant G/A snv 1.2E-05 2
rs402691
PRKCG
19 53888383 intron variant T/C snv 0.39 2
rs9990174
SLC6A1
1.000 0.040 3 10998753 intron variant G/T snv 0.31 2
rs1170695
SLC6A1 ; SLC6A1-AS1
1.000 0.040 3 11013652 5 prime UTR variant A/G snv 0.35 2
rs2944366
SLC6A1 ; SLC6A1-AS1
1.000 0.040 3 11011556 intron variant T/C snv 0.25 2