Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10503253
CSMD1
0.851 0.040 8 4323322 intron variant C/A snv 0.18 5
rs10503256
CSMD1
1.000 0.040 8 4356657 intron variant A/G snv 0.57 1
rs10503899
NRG1 ; NRG1-IT1
1.000 0.040 8 32089718 intron variant A/G snv 0.33 1
rs10509852 1.000 0.040 10 107815336 intron variant C/A;T snv 1
rs1051061
VRK2
1.000 0.040 2 58089679 missense variant A/G snv 0.36 0.31 1
rs10510653
OSBPL10
1.000 0.040 3 32017067 intron variant T/A snv 0.23 1
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 11
rs1051931
PLA2G7
0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 1
rs10520163
CLCN3
1.000 0.040 4 169705401 intron variant T/A;C snv 2
rs1054442
DDN
0.925 0.040 12 48995537 3 prime UTR variant A/C snv 0.46 4
rs1055569
HCG26 ; HCP5
0.882 0.240 6 31472305 non coding transcript exon variant C/T snv 0.41 2
rs105633
DELE1 ; PCDH12
0.882 0.040 5 141945684 synonymous variant T/C;G snv 0.98; 4.0E-06 3
rs1057518913
EHMT1
0.851 0.320 9 137762822 splice donor variant T/C snv 7
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 7
rs1064395
NCAN
0.882 0.120 19 19250926 3 prime UTR variant G/A snv 0.24 1
rs1064627
FLOT1
1.000 0.040 6 30730764 non coding transcript exon variant A/G snv 0.17 0.19 1
rs10650434
MAD1L1
1.000 0.040 7 1985461 intron variant -/TC delins 0.57 1
rs1065852
NDUFA6-DT ; LOC112268294 ; CYP2D6
0.695 0.360 22 42130692 missense variant G/A snv 0.21 0.19 2
rs1065861
MEF2C
1.000 0.040 5 88796133 intron variant A/G;T snv 1
rs10744422
HIP1R
1.000 0.040 12 122852242 intron variant T/C snv 0.85 1
rs10745841
LOC101928937 ; ANKS1B
1.000 0.040 12 99099957 intron variant G/C;T snv 0.54 1
rs10750450
LINC02551
1.000 0.040 11 130849166 intron variant G/T snv 0.58 1
rs10750489
NTM
1.000 0.040 11 131786445 intron variant C/G;T snv 0.91 1
rs1075195 1.000 0.040 20 38718108 intergenic variant T/C snv 0.76 1
rs10752262
CAMK1D
1.000 0.040 10 12353101 intron variant C/T snv 0.39 3