Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs560426
ABCA4
0.851 0.200 1 94087882 intron variant C/T snv 0.53 5
rs739439
SLC46A1 ; SARM1
0.851 0.200 17 28396803 3 prime UTR variant C/T snv 0.13 5
rs4791331
NTN1
0.925 0.120 17 9028765 intron variant C/T snv 0.53 3
rs3821949
MSX1
1.000 0.080 4 4858675 upstream gene variant G/A snv 0.32 2
rs1546124
CRISPLD2
0.807 0.200 16 84838445 5 prime UTR variant G/A;C snv 8.6E-06; 0.67 7
rs2235375
IRF6
0.807 0.400 1 209792242 intron variant G/A;C;T snv 3.2E-05; 0.41; 4.3E-04 7
rs10130587
BMP4
0.851 0.200 14 53952392 intron variant G/C snv 0.45 5
rs397515445
FGFR1
0.807 0.280 8 38414263 missense variant T/C snv 7
rs13041247
LOC102724968
0.851 0.200 20 40640434 regulatory region variant T/C snv 0.36 5
rs2239907
SARM1 ; SLC46A1
0.851 0.200 17 28398728 3 prime UTR variant T/C snv 0.53 5
rs2269529
MYH9 ; MIR6819
0.851 0.200 22 36288308 missense variant T/C snv 0.26 0.18 5
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306