Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 28
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 21
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 6
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 4
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 4
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 3
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 3
rs117834366
CNTNAP2
0.925 0.120 7 147937799 intron variant G/A snv 1.2E-02 2
rs1799990
PRNP
0.683 0.440 20 4699605 missense variant A/G snv 0.31 0.33 2
rs12007229 1.000 0.120 X 67528513 upstream gene variant C/A snv 0.11 1
rs2497931 1.000 0.120 X 67436434 intergenic variant A/C;T snv 1
rs4485213 1.000 0.120 13 105256524 intergenic variant C/T snv 0.19 1
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 1
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 1
rs10491487
RASGRF2
1.000 0.120 5 81027549 intron variant T/G snv 8.2E-02 1
rs26906
RASGRF2
1.000 0.120 5 81069068 intron variant T/C snv 0.86 1
rs290227
SYK
1.000 0.120 9 90874382 intron variant G/A snv 0.30 1
rs1800470
TGFB1
0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 1