Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4326755
TRPC6
1.000 0.120 11 101578627 intron variant G/A snv 0.48 1
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs17830558
PLA2R1
1.000 0.120 2 160021853 intron variant T/G snv 0.39 1
rs35771982
PLA2R1
0.925 0.120 2 160028907 missense variant G/C snv 0.39 0.35 2
rs4664308
LOC105373717 ; PLA2R1
0.851 0.160 2 160060986 intron variant A/G snv 0.30 4
rs3024912
LOC105373805
0.925 0.120 2 191028361 intron variant A/C snv 0.29 2
rs3024908
STAT4 ; LOC105373805
1.000 0.120 2 191029415 intron variant T/C snv 9.7E-02 1
rs3024877
STAT4
1.000 0.120 2 191040163 intron variant C/T snv 0.35 1
rs1800796
IL6-AS1 ; STEAP1B ; IL6
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs3132580
HCG21 ; SFTA2 ; MUCL3
0.790 0.360 6 30952347 missense variant G/A snv 8.0E-02 9.3E-02 7
rs3130544 0.807 0.360 6 31090563 intergenic variant C/A snv 7.4E-02 10
rs2233956
PSORS1C1 ; C6orf15
0.827 0.320 6 31113428 upstream gene variant T/C snv 0.12 5
rs3130564
PSORS1C1
0.790 0.360 6 31133897 intron variant C/T snv 0.14 7
rs7750641
TCF19
0.807 0.360 6 31161533 missense variant C/T snv 7.0E-02 7.6E-02 6
rs1265159
POU5F1
0.882 0.240 6 31172270 intron variant G/A snv 0.21 3
rs3134792
HLA-B
0.851 0.280 6 31344549 intron variant T/G snv 8.8E-02 4
rs3115663
PRRC2A ; MIR6832
0.827 0.360 6 31634066 non coding transcript exon variant T/C snv 0.17 7
rs9267522
PRRC2A
1.000 0.120 6 31635993 synonymous variant A/G snv 1
rs3130618
CSNK2B ; GPANK1
0.827 0.360 6 31664357 missense variant C/A;T snv 0.15; 4.0E-06 7
rs652888
EHMT2-AS1 ; EHMT2 ; LOC107986588 ; CYP21A2
0.776 0.480 6 31883457 non coding transcript exon variant A/G snv 0.18 0.20 10
rs389884
STK19 ; CYP21A2 ; DXO
0.776 0.440 6 31973120 non coding transcript exon variant A/G snv 7.1E-02 10
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs3096697
PPT2-EGFL8 ; PPT2 ; EGFL8
0.882 0.200 6 32166733 missense variant G/A snv 0.16 0.18 3
rs3134945
RNF5 ; MIR6833 ; AGPAT1
0.827 0.240 6 32178715 intron variant C/A snv 0.18 6