Disease: Blood Protein Measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 22
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 18
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 16
rs17863787
UGT1A9 ; UGT1A8 ; UGT1A6 ; UGT1A7 ; UGT1A10
0.925 0.040 2 233702448 intron variant T/G snv 0.30 9
rs1801020
GRK6 ; F12 ; SLC34A1
1.000 0.040 5 177409531 5 prime UTR variant A/G snv 0.65 0.67 8
rs5128
APOC3
0.925 0.080 11 116832924 3 prime UTR variant G/C snv 0.84 0.87 8
rs217181
TXNL4B
16 72080103 intron variant C/T snv 0.20 6
rs4665710 2 20998163 downstream gene variant A/C snv 0.76 6
rs11552708
TNFSF12-TNFSF13 ; TNFSF13
0.882 0.240 17 7559238 missense variant G/A;C snv 0.13; 4.2E-06 5
rs2280401
SNORD35B ; RPS11
19 49496752 intron variant G/A snv 0.12 5
rs2545801
GRK6
5 177414338 intron variant T/C snv 0.56 5
rs4985726
TNFRSF13B
0.925 0.120 17 16960324 intron variant C/G snv 0.11 5
rs174530
MYRF ; TMEM258
1.000 0.080 11 61779120 non coding transcript exon variant A/G snv 0.30 4
rs34042070
TXNL4B ; HPR
16 72067626 intron variant C/G snv 0.17 4
rs483082
APOC1
1.000 0.080 19 44912921 non coding transcript exon variant G/T snv 0.28 4
rs75759936 4 78698045 intergenic variant C/A snv 5.0E-03 3
rs2731673
GRK6
5 177412897 intron variant T/C snv 0.66 2
rs2731674
GRK6
5 177412889 intron variant T/G snv 0.66 2
rs3775298
KLKB1
4 186229324 intron variant A/G snv 0.59 2