Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs569550
LSP1
0.925 0.080 11 1865838 intron variant T/G snv 0.35 4
rs7086803
VTI1A
0.763 0.160 10 112738717 intron variant G/A snv 0.20 4
rs7223535
ATAD5
1.000 0.080 17 30884649 intron variant G/A snv 0.25 4
rs10995190
ZNF365
0.882 0.080 10 62518923 intron variant G/A snv 0.16 3
rs11249433
EMBP1
0.827 0.160 1 121538815 intron variant A/C;G snv 3
rs117758012
HOOK2 ; MAST1
1.000 0.080 19 12846836 intron variant C/T snv 4.1E-02 3
rs1219648
FGFR2
0.716 0.320 10 121586676 intron variant A/G;T snv 3
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 3
rs12405132
RNF115
0.882 0.200 1 145790097 intron variant G/A snv 0.29 3
rs13281615
CASC8 ; POU5F1B ; PCAT1 ; CASC21
0.716 0.360 8 127343372 intron variant A/G snv 0.43 3
rs13431652
SPC25
0.925 0.080 2 168896905 intron variant T/C snv 0.24 3
rs1353747
PDE4D
0.882 0.080 5 59041654 intron variant T/G snv 6.9E-02 3
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 3
rs17021918
PDLIM5
0.776 0.240 4 94641726 intron variant C/T snv 0.30 3
rs17356907
PGAM1P5
0.925 0.080 12 95633983 intron variant A/G snv 0.28 3
rs1858826
GNGT1
1.000 0.080 7 93719703 intron variant C/T snv 0.90 3
rs1973765
LSP1
1.000 0.080 11 1877434 intron variant T/C snv 0.37 3
rs2075555
COL1A1
0.807 0.240 17 50196930 intron variant T/A;G snv 3
rs2180341
RNF146
0.882 0.160 6 127279485 intron variant G/A snv 0.73 3
rs2188380
LINC01405
0.851 0.200 12 110948323 intron variant T/C snv 4.7E-03 3
rs2242652
TERT
0.724 0.400 5 1279913 intron variant G/A snv 0.18 3
rs2284378
RALY
0.851 0.080 20 34000289 intron variant T/C;G snv 3
rs2435357
RET
0.790 0.240 10 43086608 intron variant T/C snv 0.79 3
rs2981582
FGFR2
0.695 0.360 10 121592803 intron variant A/G snv 0.58 3
rs3218020
CDKN2B-AS1
0.882 0.120 9 21997873 intron variant G/A;C snv 3