Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs371609024
FUT8
0.925 0.120 14 65629530 missense variant A/G snv 4.0E-06 2
rs3729587
XPC
0.925 0.120 3 14167125 intron variant G/C snv 0.31 0.34 2
rs3731055
XPC ; LSM3
0.925 0.120 3 14178939 intron variant C/T snv 1.9E-02 2
rs3731114
XPC
0.925 0.120 3 14165122 intron variant C/G snv 1.8E-02 2
rs3751936
RPTOR
0.925 0.120 17 80964404 3 prime UTR variant G/C snv 0.20 2
rs4149086
SLCO1B1
0.925 0.120 12 21239517 3 prime UTR variant A/G snv 4.5E-04 2
rs4795218
HNF1B ; LOC105371754
0.925 0.120 17 37718512 intron variant A/G snv 0.82 2
rs488087
CEL
0.925 0.120 9 133071212 synonymous variant C/A;T snv 0.11 0.26 2
rs4927850
TFRC
0.925 0.120 3 196024759 intron variant T/C snv 0.71 2
rs4988487
SSTR5 ; SSTR5-AS1
0.925 0.120 16 1079193 missense variant C/A;T snv 4.0E-06; 5.3E-02 2
rs5757573
PDGFB
0.925 0.120 22 39237617 intron variant C/T snv 0.57 2
rs5768709
TAFA5
0.925 0.120 22 48533757 intron variant A/G snv 0.36 2
rs6001516 0.925 0.120 22 39248198 intron variant C/T snv 6.1E-02 2
rs6127119
CYP24A1
0.925 0.120 20 54162543 intron variant C/T snv 0.24 2
rs62068300
RPTOR
0.925 0.120 17 80600927 intron variant G/A;T snv 5.7E-05 2
rs6464375
DPP6
0.925 0.120 7 153928758 intron variant C/T snv 6.7E-02 2
rs6475609
CDKN2B-AS1
0.925 0.120 9 22106272 intron variant A/C;G;T snv 2
rs7074891
TRDMT1
0.925 0.120 10 17146475 3 prime UTR variant C/T snv 0.95 2
rs708224
BICD1
0.925 0.120 12 32283475 intron variant A/G snv 0.50 2
rs747601652
CRYZ
0.925 0.120 1 74723233 missense variant A/G snv 1.2E-05 2
rs767964519
NFE2L2
0.925 0.120 2 177231869 missense variant T/C snv 4.0E-06 2
rs779731636
SOD2
0.925 0.120 6 159685026 missense variant C/A snv 8.6E-06 2
rs782095550
MANF
0.925 0.120 3 51386267 missense variant T/C snv 2
rs782128510
C17orf97 ; LOC105371430
0.925 0.120 17 410373 missense variant C/A;G snv 7.6E-05; 8.4E-06 2
rs78417682
TNS3
0.925 0.120 7 47449305 intron variant G/C snv 0.15 2