Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057518806
HMBS
1.000 0.040 11 119093155 frameshift variant G/- del 4
rs3761422
ADORA2A ; ADORA2A-AS1 ; SPECC1L-ADORA2A
1.000 0.040 22 24430704 intron variant T/C snv 0.62 4
rs4752856
MTCH2
1.000 0.040 11 47626490 intron variant G/A snv 0.28 4
rs4822492
ADORA2A-AS1
1.000 0.040 22 24447626 intron variant C/G snv 0.47 4
rs1110976
DRD2
1.000 0.040 11 113413797 intron variant T/G snv 3
rs1132358
BAIAP3
1.000 0.040 16 1347814 synonymous variant C/T snv 0.44 0.39 3
rs13262595
LOC107986983 ; TSNARE1
1.000 0.040 8 142235609 intron variant A/C;G snv 3
rs1426371
LOC105369965 ; WSCD2
1.000 0.040 12 108236003 intron variant G/A snv 0.20 3
rs17536211
GABRG1
1.000 0.040 4 46085716 intron variant A/C snv 0.14 3
rs2180619
CNR1
1.000 0.040 6 88168233 upstream gene variant G/A snv 0.53 3
rs2235632
BAIAP3
1.000 0.040 16 1343019 splice region variant G/A snv 0.46 0.42 3
rs3812047
GDNF-AS1 ; GDNF
1.000 0.040 5 37835296 intron variant C/G;T snv 3
rs7528604
PDE4B
0.925 0.040 1 65941669 intron variant G/A snv 0.42 3
rs10507274
C12orf49
1.000 0.040 12 116723171 missense variant T/C snv 4.7E-02 4.4E-02 2
rs11090045
ZC3H7B
1.000 0.040 22 41357599 3 prime UTR variant G/A;C snv 2
rs112146896
EFHD2
1.000 0.040 1 15418527 intron variant A/C;G;T snv 2
rs1248860
CADM2
1.000 0.040 3 84966628 intron variant G/A snv 0.56 2
rs12765002
AS3MT ; BORCS7-ASMT
1.000 0.040 10 102875591 intron variant C/T snv 0.24 2
rs1277240795
OGA
1.000 0.040 10 101791382 missense variant G/C snv 7.0E-06 2
rs1960264
LOC105373148 ; SAT1
1.000 0.040 X 23781758 intron variant C/G;T snv 2
rs2572431 1.000 0.040 8 11247568 downstream gene variant C/G;T snv 2
rs2941026
CCKBR
1.000 0.040 11 6261042 intron variant A/G snv 0.51 2
rs2973050
GDNF-AS1 ; GDNF
1.000 0.040 5 37817242 intron variant A/G;T snv 2
rs3026401
PAX6 ; ELP4
1.000 0.040 11 31785976 3 prime UTR variant C/T snv 0.71 2
rs34548976 1.000 0.040 7 31032854 intergenic variant C/T snv 0.39 2