Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4773144
COL4A1 ; COL4A2
0.827 0.080 13 110308365 intron variant A/G snv 0.42 7
rs734553
SLC2A9
0.851 0.240 4 9921380 intron variant G/A;T snv 7
rs881858
LOC105375069 ; LOC107986598
0.882 0.200 6 43838872 intron variant G/A;C snv 7
rs968567
FADS2 ; FADS1
0.851 0.240 11 61828092 intron variant C/T snv 0.11 7
rs1171616
SLC16A9
0.882 0.200 10 59708831 intron variant G/T snv 0.79 6
rs6495446
MTHFS ; ST20-MTHFS
0.851 0.200 15 79862640 intron variant C/T snv 0.31 6
rs7901695
TCF7L2
0.851 0.160 10 112994329 intron variant T/C snv 0.34 6
rs10109414 1.000 0.080 8 23893638 regulatory region variant C/T snv 0.37 5
rs12373237
LAMA3
0.851 0.200 18 23845972 intron variant G/A snv 0.47 5
rs12922822
UMOD
1.000 0.040 16 20356323 upstream gene variant C/A;T snv 5
rs13038305
CST3
0.925 0.080 20 23629625 intron variant C/T snv 0.21 5
rs17319721
SHROOM3
0.925 0.080 4 76447694 intron variant G/A snv 0.34 5
rs174545
FADS1 ; FADS2
1.000 0.080 11 61801834 3 prime UTR variant C/A;G snv 0.28 5
rs174560
FADS1 ; FADS2
1.000 0.080 11 61814292 non coding transcript exon variant T/C snv 0.30 5
rs2569512
ILF3
0.925 0.080 19 10679486 intron variant T/C snv 0.76 5
rs28456
FADS1 ; FADS2
0.925 0.120 11 61822009 intron variant A/C;G snv 5
rs5854292
EGFEM1P
0.851 0.080 3 168680960 intron variant AA/-;A;AAA delins 5
rs626277
DACH1
1.000 0.080 13 71773564 intron variant A/C snv 0.51 5
rs6420094
SLC34A1
1.000 0.080 5 177390635 intron variant A/G snv 0.29 5
rs7394579
FADS2 ; FADS1
1.000 0.080 11 61813978 intron variant A/G snv 0.22 5
rs7805747
PRKAG2
1.000 0.080 7 151710715 intron variant G/A snv 0.26 5
rs97384
FADS2
1.000 0.080 11 61856709 non coding transcript exon variant T/C snv 0.46 5
rs10774021
SLC6A13
1.000 0.080 12 240132 intron variant C/T snv 0.57 4
rs10794720
WDR37
1.000 0.080 10 1110225 intron variant T/C snv 0.89 4
rs112329286
SYNE2
1.000 0.080 14 63773159 intron variant -/ATTT delins 0.24 4