Disease: Heart failure
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs958546
LRRC63
0.882 0.040 13 46259582 intron variant G/C snv 0.29 3
rs2549513
MAF
0.851 0.080 16 79516830 downstream gene variant C/A;T snv 4
rs499818 0.851 0.080 6 13332235 upstream gene variant G/A snv 0.21 4
rs9351814 0.882 0.040 6 71484004 intergenic variant A/C snv 0.35 4
rs740363
HSPA12A
0.851 0.080 10 116816095 intron variant G/A snv 0.40 5
rs16867253
GRHL1
0.851 0.120 2 9956965 intron variant G/T snv 5.8E-02 7
rs460976 0.851 0.120 21 41463567 downstream gene variant A/G;T snv 7
rs7081476
ANKRD26
0.851 0.120 10 26969741 intergenic variant G/C;T snv 7
rs911119
CST3
0.807 0.120 20 23632100 non coding transcript exon variant C/G;T snv 9
rs1320702652
MFAP1
0.752 0.160 15 43824536 missense variant G/A snv 4.0E-06 11
rs1799998
CYP11B2
0.742 0.200 8 142918184 upstream gene variant A/G;T snv 0.38 14
rs12310617 0.851 0.120 12 3060327 intergenic variant C/T snv 0.11 16
rs12369179
ZCCHC8
0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02 16
rs12420422 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 16
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs17140821 0.851 0.120 7 19177581 regulatory region variant G/A snv 7.9E-02 16
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14 16
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16
rs2866611 0.851 0.120 20 41322165 upstream gene variant A/T snv 0.58 16
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs3798220
LPA
0.732 0.160 6 160540105 missense variant T/C snv 5.6E-02 3.1E-02 16
rs4704221
CERT1
0.851 0.120 5 75463358 intron variant T/A;C snv 16
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv 16
rs6533530 0.851 0.120 4 110810780 intergenic variant T/C snv 0.47 16
rs6759518
SLC30A3
0.851 0.120 2 27263727 intron variant G/C snv 5.5E-02 16