Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs5361
SELE ; C1orf112
0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs12212067
FOXO3
0.716 0.320 6 108659993 intron variant T/G snv 0.14 20
rs6136
SELP
0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 17
rs76895963
CCND2-AS1 ; CCND2
1.000 0.080 12 4275678 intron variant T/G snv 1.5E-02 6
rs1408888
DACH1
0.851 0.120 13 71854515 intron variant T/G snv 0.30 5
rs62434109
PLEKHG1
6 150654176 intron variant T/G snv 8.4E-02 5
rs71636784
ZDHHC18
1.000 0.040 1 26842709 intron variant T/G snv 0.12 4
rs72831343
CABCOCO1
10 61755923 intron variant T/G snv 9.3E-02 2
rs10850407 12 114940232 intergenic variant T/G snv 0.24 1
rs13285624
ZCCHC7
9 37129499 intron variant T/G snv 0.33 1
rs188315257
DNAJC27-AS1
2 25018517 intron variant T/G snv 5.6E-02 1
rs2478981 20 63852557 intergenic variant T/G snv 0.57 1
rs2977324 8 75804502 intergenic variant T/G snv 0.77 1
rs41316468
MIR6842 ; PTK2B
8 27432501 intron variant T/G snv 7.4E-03 1
rs7267618
ZNF831
20 59131469 intron variant T/G snv 0.11 1
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs2241766
ADIPOQ ; ADIPOQ-AS1
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs12916
HMGCR ; CERT1
0.807 0.240 5 75360714 3 prime UTR variant T/C;G snv 0.37 12
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 10
rs1801239
CUBN
0.827 0.160 10 16877053 missense variant T/C;G snv 8.9E-02; 8.0E-06 8
rs5050
AGT
0.827 0.200 1 230714140 intron variant T/C;G snv 7
rs1537375
CDKN2B-AS1
0.882 0.120 9 22116072 intron variant T/C;G snv 6
rs112684153
MTRF1
13 41275595 intergenic variant T/C;G snv 1