Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9470361 0.776 0.080 6 36655602 regulatory region variant G/A;T snv 12
rs35107139
BMP4
0.776 0.080 14 53952388 intron variant A/C;G;T snv 11
rs4939827
SMAD7
0.708 0.160 18 48927093 intron variant T/A;C snv 11
rs1078643
TMEM220-AS1 ; TMEM238L
0.776 0.080 17 10803924 missense variant G/A;C snv 10
rs11150038
CLEC3A
0.790 0.080 16 78042662 intron variant A/C;G snv 10
rs11196170
TCF7L2
0.776 0.080 10 112962862 intron variant G/A;C snv 10
rs11610543 0.776 0.080 12 42740389 intergenic variant A/G;T snv 10
rs121913412
CTNNB1
0.724 0.280 3 41224633 missense variant A/C;G;T snv 10
rs17102823 0.776 0.080 14 34894698 intergenic variant A/C;G snv 10
rs189583 0.776 0.080 20 6395810 regulatory region variant G/C;T snv 10
rs1963413
TMEM91 ; B9D2
0.776 0.080 19 41365668 intron variant G/A;C;T snv 10
rs2250430
PLEKHG6
0.776 0.080 12 6312008 intron variant A/C;T snv 10
rs2293581
GREM1 ; LOC100131315
0.776 0.080 15 32718535 5 prime UTR variant G/A;C snv 0.27 10
rs34405347 0.776 0.080 9 98917470 regulatory region variant T/C;G snv 10
rs45597035
KLF5
0.776 0.080 13 73075014 intron variant A/G;T snv 10
rs4968127
NXN
0.776 0.080 17 906403 intron variant G/A;T snv 10
rs6066825
PREX1
0.776 0.080 20 48723580 intron variant A/G;T snv 10
rs61389091
CHRDL2
0.776 0.080 11 74716876 intron variant C/G;T snv 10
rs6678517
LAMC1
0.776 0.080 1 183033504 intron variant A/G;T snv 10
rs7121958
POLD3
0.776 0.080 11 74568967 intron variant T/A;G snv 10
rs7708610 0.776 0.080 5 40102341 intergenic variant G/A;C snv 10
rs7758229
SLC22A3
0.732 0.120 6 160419220 intron variant G/A;T snv 10
rs9901225
RETREG3
0.790 0.080 17 42603793 intron variant C/G;T snv 10
rs9930005 0.776 0.080 16 80009361 intergenic variant C/A;T snv 10
rs10152518 0.790 0.080 15 67884824 intergenic variant G/A;T snv 9