Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1385600
USP35 ; GAB2
0.925 0.080 11 78225120 synonymous variant A/G snv 0.25 0.27 2
rs5984894
PCDH11X
0.925 0.080 X 92138738 intron variant A/G snv 0.54 2
rs6691117
CR1
1.000 0.080 1 207609586 missense variant A/G snv 0.32 0.41 2
rs7101429
GAB2
0.925 0.080 11 78281921 intron variant A/G snv 0.15 2
rs7764257
TTBK1
0.925 0.080 6 43257017 intron variant A/G snv 0.32 2
rs802571
CNTNAP2
0.925 0.080 7 146265094 intron variant A/G snv 0.22 2
rs9340803
ESR1
0.925 0.080 6 151842832 intron variant A/G snv 1.0E-03 3.8E-04 2
rs10197851
HPCAL1
1.000 0.080 2 10345283 intron variant A/G snv 0.52 1
rs10410711
ZNF566
1.000 0.080 19 36449796 synonymous variant A/G snv 3.3E-02 3.5E-02 1
rs116754410
CD2AP
1.000 0.080 6 47624205 missense variant A/G snv 2.1E-03 8.3E-03 1
rs116806486
CR1
1.000 0.080 1 207523640 missense variant A/G snv 1.6E-03 5.4E-03 1
rs2160525
LRP6 ; BCL2L14
1.000 0.080 12 12117356 3 prime UTR variant A/G snv 0.82 1
rs2279420 1.000 0.080 10 60022189 downstream gene variant A/G snv 8.8E-02 1
rs3844508
ESR1
1.000 0.080 6 151818907 intron variant A/G snv 0.23 1
rs4646955
IDE
1.000 0.080 10 92534534 intron variant A/G snv 0.21 0.20 1
rs4669573
HPCAL1
1.000 0.080 2 10338810 intron variant A/G snv 0.47 1
rs67327804
BIN1
1.000 0.080 2 127069056 intron variant A/G snv 0.30 0.33 1
rs7179008
CHRNA7
1.000 0.080 15 32151722 intron variant A/G snv 0.22 1
rs770461695
PICALM
1.000 0.080 11 85981991 missense variant A/G snv 1.6E-05 1
rs950809
SORCS1
1.000 0.080 10 107035617 intron variant A/G snv 0.48 1
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1550117
DNMT3A
0.790 0.320 2 25343038 upstream gene variant A/G;T snv 11
rs6656401
CR1
0.776 0.200 1 207518704 intron variant A/G;T snv 8
rs2718058
EPDR1 ; GPR141
0.925 0.080 7 37801932 intron variant A/G;T snv 2
rs63750215
PSEN2
0.701 0.240 1 226885603 missense variant A/T snv 19