Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9862857
LOC101927995 ; LOC105377013
0.851 0.040 3 30453840 regulatory region variant A/G;T snv 4
rs9825823
FHIT
0.851 0.080 3 61096480 intron variant T/C snv 0.47 2
rs9364726 0.882 0.040 6 164236705 intergenic variant A/G snv 6.5E-02 3
rs9321987
UTRN
0.925 0.040 6 144709148 intron variant C/T snv 0.40 3
rs853679
ZSCAN31
0.851 0.160 6 28329086 intron variant C/A snv 0.20 4
rs80278479
TFAP2D
0.925 0.040 6 50758466 intron variant C/G snv 3.0E-03 3
rs7973260
KSR2
0.851 0.120 12 117937681 intron variant A/G snv 0.83 2
rs7828021 0.925 0.040 8 49727454 intergenic variant C/G;T snv 3
rs782212
LOC105378797
0.925 0.040 1 72479983 intron variant C/T snv 0.34 2
rs78087832 0.925 0.040 2 224600060 intergenic variant C/T snv 2.4E-03 3
rs77945277
BAZ1A
0.925 0.040 14 34840969 intron variant A/G snv 4.9E-03 3
rs77826363 0.882 0.040 6 1128802 intergenic variant G/T snv 2.2E-02 3
rs76767803 0.925 0.040 3 36230378 intergenic variant C/T snv 0.16 2
rs760161369
MTHFR
0.882 0.040 1 11800214 missense variant G/A;C snv 2.8E-05; 4.0E-06 1
rs75995702 0.925 0.040 11 42785177 intergenic variant C/G;T snv 3
rs75921243 0.925 0.040 8 9988356 intron variant T/G snv 1.9E-02 2
rs7555693 0.925 0.040 1 106295917 intergenic variant G/A snv 0.45 3
rs74860738 0.925 0.040 11 80671683 intergenic variant G/A snv 7.2E-02 3
rs73425402
NAV3
0.925 0.040 12 77503518 intron variant T/A snv 4.1E-02 3
rs7189979
SNX29
0.925 0.040 16 12536330 intron variant A/C;G;T snv 3
rs6740584
CREB1
0.882 0.040 2 207564627 intron variant T/C snv 0.37 1
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 4
rs6586354 0.851 0.040 1 234897489 intron variant G/A snv 0.25 4
rs6546604 0.925 0.040 2 70415675 intron variant G/A;T snv 3
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 8