Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1937863
AKR1C2
0.925 0.080 10 5009340 intron variant G/A;C;T snv 3
rs2133450
GRM7
0.925 0.080 3 7294765 intron variant A/C snv 0.38 3
rs2793094
TSNAX-DISC1 ; DISC1
0.925 0.080 1 231741236 intron variant G/A snv 0.97 3
rs33990840
AVPR1B
0.925 0.080 1 206116320 missense variant C/G;T snv 5.0E-02; 2.8E-05 3
rs4658966
DISC1 ; TSNAX-DISC1 ; DISC1-IT1
0.925 0.080 1 231942868 intron variant T/C snv 0.19 3
rs553040076
CDC37 ; PDE4A
0.925 0.080 19 10417700 missense variant T/A snv 4.5E-05 7.7E-05 3
rs5558
SLC6A2
0.925 0.080 16 55699647 missense variant T/G snv 3
rs6704393
NOS1AP
0.925 0.080 1 162182266 intron variant C/A;T snv 3
rs747052707
FOLH1
0.925 0.080 11 49192822 missense variant T/C snv 2.4E-05; 8.1E-06 3
rs7486220
TIMELESS
0.925 0.080 12 56443632 intron variant C/T snv 3
rs8192625
TAAR6
0.925 0.080 6 132571193 missense variant G/A snv 6.2E-02 7.8E-02 3
rs9376026
SGK1
0.925 0.080 6 134281316 intron variant T/C snv 0.43 3
rs977605156
DNASE1 ; TRAP1
0.925 0.080 16 3656127 missense variant G/A snv 7.0E-06 3
rs57875989
PER3
0.882 0.080 1 7829913 splice acceptor variant GCTCTGTCCACAGGATCGCCTCCCATGAAGAATCCATCCCATCCTACTGCCAGC/-;GCTCTGTCCACAGGATCGCCTCCCATGAAGAATCCATCCCATCCTACTGCCAGCGCTCTGTCCACAGGATCGCCTCCCATGAAGAATCCATCCCATCCTACTGCCAGC delins 0.11 0.18 7
rs1409851868
EPHA3
0.882 0.080 3 89399325 missense variant A/G snv 6
rs11111
GDNF-AS1 ; GDNF
0.882 0.080 5 37814000 3 prime UTR variant T/C snv 0.22 5
rs1187323
NTRK2
0.882 0.080 9 84668501 upstream gene variant C/A;G;T snv 5
rs1220000453
ZFP91-CNTF ; CNTF
0.882 0.120 11 58624189 synonymous variant C/T snv 5
rs13440581
GPR50
0.882 0.080 X 151181399 missense variant A/G snv 0.45 0.45 5
rs2070587
DAO
0.882 0.080 12 108883967 intron variant T/G snv 0.32 5
rs2072115
RAPGEF3
0.882 0.080 12 47751585 intron variant A/C;G snv 5
rs228697
PER3
0.882 0.080 1 7827519 missense variant C/G snv 8.7E-02 7.3E-02 5
rs3096140
GDNF ; GDNF-AS1
0.882 0.080 5 37832731 intron variant G/A snv 0.69 5
rs3782218
NOS1
0.882 0.120 12 117333706 intron variant C/T snv 0.19 5
rs884344
GDNF ; GDNF-AS1
0.882 0.120 5 37824138 intron variant A/C snv 0.33 5