Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4919510
SEMA4G ; MIR608 ; MRPL43
0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27 32
rs116671518
DKK2
4 107189709 intron variant T/C snv 1.9E-02 1
rs6797827 3 109735523 intron variant C/T snv 0.18 1
rs80274284
SLC22A15
1 116037356 missense variant G/T snv 1
rs5861895 4 129344228 regulatory region variant TT/-;T;TTT delins 1
rs1048369
GPC4
0.882 0.160 X 133303309 missense variant G/A snv 0.33 0.38 4
rs62309385 4 136134743 intron variant G/C snv 9.8E-02 1
rs6105452
MACROD2
20 15683126 intron variant C/T snv 0.10 1
rs200655768
TTN-AS1 ; TTN
2 178711222 synonymous variant G/A;T snv 1
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs314879 13 22735243 intergenic variant C/T snv 0.78 1
rs12759054
SLC35F3
1.000 0.040 1 233984064 intron variant T/A;C snv 3
rs1062630
POU5F1
6 31170330 synonymous variant G/A snv 0.18 0.22 1
rs3130070
PRRC2A
6 31624031 intron variant A/G snv 0.17 1
rs3130623
PRRC2A
6 31629923 intron variant C/T snv 0.18 1
rs3130626
PRRC2A
1.000 0.120 6 31630712 synonymous variant A/G snv 0.15 0.17 2
rs2736157
MIR6832 ; PRRC2A
1.000 0.120 6 31633043 intron variant A/G;T snv 0.15 0.17 2
rs3115663
PRRC2A ; MIR6832
0.827 0.360 6 31634066 non coding transcript exon variant T/C snv 0.17 7
rs11229
PRRC2A
0.851 0.280 6 31635993 synonymous variant A/G snv 0.14 0.17 6
rs10885
PRRC2A
6 31636814 missense variant C/T snv 0.14 0.17 1
rs3130628
BAG6
1.000 0.120 6 31641495 non coding transcript exon variant T/C snv 0.15 0.18 2
rs3130048
BAG6
1.000 0.120 6 31645962 intron variant T/C snv 0.23 3
rs3117583
APOM ; BAG6
0.925 0.200 6 31651799 5 prime UTR variant A/G snv 0.14 0.17 3
rs3130618
CSNK2B ; GPANK1
0.827 0.360 6 31664357 missense variant C/A;T snv 0.15; 4.0E-06 7
rs9267532
LY6G5B ; CSNK2B
1.000 0.120 6 31672202 missense variant C/T snv 7.4E-02 7.9E-02 2