Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs773941026
FGF14
1.000 13 102401633 missense variant A/G;T snv 2.4E-05 1
rs121908160
KIF1B
0.882 0.080 1 10258602 missense variant A/T snv 4
rs39399
RELN
0.925 0.040 7 103849545 intron variant G/A;T snv 2
rs1048103951
TXNRD1
0.925 0.040 12 104321282 missense variant G/A snv 2
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 39
rs769142993
ATM ; C11orf65
0.851 0.280 11 108331498 missense variant G/C;T snv 2.4E-05 7.0E-06 7
rs397514624
COL4A1
0.925 13 110187254 missense variant G/A;C;T snv 1.6E-05; 4.0E-06 3
rs200786329
COL4A1
0.925 13 110201467 missense variant G/A snv 5.2E-05 1.7E-04 3
rs4884357
TARDBP
0.807 0.120 1 11022301 missense variant G/A;T snv 4.0E-06 6
rs80356740
TARDBP
1.000 1 11022556 missense variant A/G snv 1.7E-05 2
rs879254382
LDLR
0.882 0.080 19 11089549 start lost A/C;G;T snv 3
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs781902168
HSPB2 ; CRYAB ; HSPB2-C11orf52
0.882 0.040 11 111911694 missense variant G/A;C snv 3.2E-05 3
rs1420960657
SDHD
0.851 0.080 11 112093192 missense variant A/G snv 4
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins 36
rs1801155
APC
0.649 0.440 5 112839514 missense variant T/A snv 8.0E-06; 2.0E-03 1.2E-03 42
rs1801166
APC
0.732 0.200 5 112839543 missense variant G/C snv 4.4E-03 5.6E-03 17
rs1800497
ANKK1
0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs6277
DRD2
0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs1799732
DRD2 ; LOC105369501
0.790 0.160 11 113475529 intron variant -/G delins 11
rs7080536
HABP2 ; NRAP
0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 27
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs104894073
GATA4
0.827 0.080 8 11750213 missense variant G/A;C;T snv 8
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1219648
FGFR2
0.716 0.320 10 121586676 intron variant A/G;T snv 17