Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9839376
KCNMB2 ; KCNMB2-AS1
1.000 0.040 3 178741877 intron variant T/C snv 0.18 1
rs971257
B3GALT1
1.000 0.040 2 167782126 intergenic variant A/C;T snv 0.53 1
rs9651492
PTEN
0.882 0.160 10 87933216 missense variant G/A;C snv 3
rs9635542
PPL
1.000 0.040 16 4951379 intron variant A/G snv 0.11 2
rs9608521
LOC105372976
1.000 0.040 22 26803274 intergenic variant C/T snv 0.33 1
rs936938
FYCO1 ; CXCR6
1.000 0.040 3 45939277 intron variant C/T snv 0.37 1
rs932026 1.000 0.040 18 38425547 intergenic variant G/A snv 0.14 1
rs9302952
SLC39A11
1.000 0.040 17 73068087 non coding transcript exon variant A/C snv 0.14 1
rs9293194
MSNP1
1.000 0.040 5 25911027 non coding transcript exon variant C/A snv 0.46 1
rs926938
AMPD1
1.000 0.040 1 114697195 upstream gene variant A/G;T snv 1
rs922551 1.000 0.040 5 25867431 intergenic variant A/G snv 0.28 1
rs886041116
ADNP
0.776 0.240 20 50892526 stop gained G/A snv 13
rs886040971
TRPS1
0.683 0.280 8 115604339 stop gained G/A;T snv 56
rs879255652
SCN8A
0.807 0.120 12 51790425 stop gained G/A;T snv 7
rs879254129
GRIN2B
0.925 0.040 12 13562977 missense variant A/G snv 4.0E-06 2
rs876660634
PTEN
0.807 0.200 10 87925551 missense variant A/C;G snv 10
rs869312966
SCN8A
0.827 0.120 12 51806345 missense variant G/T snv 7
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs850807 0.882 0.040 15 23652982 intergenic variant T/A;C snv 3
rs849578
NRP2
1.000 0.040 2 205738798 intron variant G/A;T snv 1
rs849563
NRP2
1.000 0.040 2 205745778 synonymous variant T/A;G snv 4.0E-06; 0.19 1
rs8453
CSDE1 ; NRAS
1.000 0.040 1 114716978 3 prime UTR variant G/T snv 0.11 1
rs841361
LOC105378860 ; SLC44A3-AS1
1.000 0.040 1 94686257 intron variant C/T snv 0.48 1
rs836474
RAC1
1.000 0.040 7 6394456 intron variant G/T snv 0.13 1
rs81002885
BRCA2
0.827 0.280 13 32316529 splice donor variant T/A;C;G snv 4.0E-06 6