Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11957829
LOC100505841
1.000 0.080 5 122179500 intron variant A/G snv 0.18 0.19 2
rs12122341 1.000 0.080 1 115113069 regulatory region variant C/G snv 0.19 2
rs12214600
KCNK17
1.000 0.080 6 39300960 intron variant C/T snv 0.14 2
rs12429692
ALOX5AP
1.000 0.080 13 30738041 intron variant A/T snv 0.24 2
rs12445022 1.000 0.080 16 87541726 intergenic variant G/A snv 0.27 2
rs1263282981
STX17-AS1 ; NR4A3
1.000 0.080 9 99828749 missense variant C/T snv 1.4E-05 2
rs1341665 1.000 0.080 1 159721769 intergenic variant G/A snv 0.32 2
rs1346452438
LY6G5B ; CSNK2B
1.000 0.080 6 31670987 missense variant G/A snv 2
rs1378577
ABCG1
1.000 0.080 21 42199555 upstream gene variant T/G snv 0.33 2
rs1406885199
HPS1
1.000 0.080 10 98433988 missense variant C/A;T snv 6.0E-06 2
rs1455404812
ACE
1.000 0.080 17 63488732 missense variant C/T snv 2
rs147270785
MASP2
1.000 0.080 1 11046616 missense variant G/A snv 6.5E-04 6.4E-04 2
rs1481280
ROCK1
1.000 0.080 18 21075490 intron variant C/A snv 0.31 2
rs1671021
LLGL2
1.000 0.080 17 75569090 missense variant T/C snv 0.36 0.50 2
rs17222919
ALOX5AP
1.000 0.080 13 30734192 intron variant T/A;G snv 2
rs17286604
KALRN
1.000 0.080 3 124233370 intron variant C/T snv 0.28 2
rs1801701
APOB
1.000 0.080 2 21005955 missense variant C/T snv 7.0E-02 6.6E-02 2
rs1804689
HPS1 ; LOC101927278
1.000 0.080 10 98445350 5 prime UTR variant G/T snv 0.28 2
rs2229383
ILF3
1.000 0.080 19 10683954 synonymous variant G/A;C;T snv 4.0E-06; 0.68 2
rs2271347
PARP1
1.000 0.080 1 226361797 non coding transcript exon variant G/A snv 0.16 2
rs2280887
ARHGEF10
1.000 0.080 8 1907598 intron variant C/G snv 0.26 2
rs2295786
SH3PXD2A
1.000 0.080 10 103856724 upstream gene variant A/G;T snv 2
rs2364368
ALDH1L1 ; ALDH1L1-AS2
1.000 0.080 3 126186237 intron variant A/T snv 0.35 2
rs238670 1.000 0.080 20 23508073 intron variant T/G snv 3.9E-02 2
rs2589998 1.000 0.080 7 138181624 intergenic variant C/T snv 0.25 2