Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4418728 10 93079967 downstream gene variant G/T snv 0.42 8
rs1801689
APOH
17 66214462 missense variant A/C;G snv 4.0E-06; 2.4E-02; 4.8E-05 7
rs333947
CSF1
1 109928142 intron variant G/A snv 0.13 7
rs11553699
TMEM120B ; RHOF
12 121779004 3 prime UTR variant A/G snv 9.4E-02 6
rs217181
TXNL4B
16 72080103 intron variant C/T snv 0.20 6
rs415895
SWAP70
11 9748015 missense variant C/G snv 0.62 0.61 6
rs4665710 2 20998163 downstream gene variant A/C snv 0.76 6
rs77303550
TXNL4B
16 72045758 intron variant C/T snv 0.19 6
rs8176747
ABO
9 133255928 missense variant C/A;G snv 4.1E-06; 0.12 6
rs1065853 19 44909976 non coding transcript exon variant G/A;C;T snv 5
rs11636952
LMAN1L
15 74821981 intron variant T/C snv 0.48 5
rs13412535
SERPINE2
2 224010157 intron variant G/A snv 0.17 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
rs438811
APOC1
19 44913484 non coding transcript exon variant C/T snv 0.29 5
rs4761234 12 69338325 TF binding site variant T/C snv 0.36 5
rs9411378
ABO
9 133270015 intron variant A/C;T snv 5
rs17315646
GALNT2
1 230159560 intron variant C/A;G snv 0.45 4
rs1958078
SMOC1
14 69888141 intron variant A/C;G snv 4
rs34042070
TXNL4B ; HPR
16 72067626 intron variant C/G snv 0.17 4
rs413141 19 6675978 downstream gene variant A/G snv 0.84 4
rs884205
TNFRSF11A
18 62387624 3 prime UTR variant A/C;T snv 4
rs9302635
DHX38
16 72110275 intron variant T/C;G snv 4
rs10418046
NLRP12
19 53824615 upstream gene variant T/G snv 0.26 3
rs1042445
HRG ; LOC105374258
3 186677647 missense variant C/A;T snv 0.27 3