Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs603424
PKD2L1
1.000 0.080 10 100315722 intron variant G/A snv 0.34 13
rs1367117
APOB
1.000 0.080 2 21041028 missense variant G/A snv 0.26 0.24 8
rs174541
FADS2
1.000 0.080 11 61798436 intron variant T/C snv 0.29 8
rs174554
FADS1 ; FADS2
1.000 0.080 11 61811991 intron variant A/G snv 0.40 0.28 7
rs174574
FADS2
1.000 0.080 11 61832870 intron variant A/C snv 0.55 7
rs3925584
LOC101928338
1.000 0.080 11 30738788 intergenic variant T/C snv 0.35 7
rs10109414 1.000 0.080 8 23893638 regulatory region variant C/T snv 0.37 5
rs12922822
UMOD
1.000 0.040 16 20356323 upstream gene variant C/A;T snv 5
rs13538
NAT8 ; ALMS1P1
1.000 0.080 2 73641201 missense variant A/G snv 0.21 0.31 5
rs174528
TMEM258 ; MYRF
1.000 0.080 11 61776027 intron variant T/C snv 0.42 0.42 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
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
rs11959928
DAB2 ; C9
1.000 0.080 5 39397030 intron variant T/A snv 0.39 4
rs12460876
SLC7A9
1.000 0.080 19 32865985 intron variant T/C snv 0.36 4
rs174530
MYRF ; TMEM258
1.000 0.080 11 61779120 non coding transcript exon variant A/G snv 0.30 4
rs174564
FADS2 ; FADS1
1.000 0.080 11 61820833 intron variant A/G snv 0.30 4
rs174567
FADS1 ; FADS2
1.000 0.080 11 61825533 intron variant A/G;T snv 4