Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1334496 1.000 0.040 X 137178554 intergenic variant C/A;T snv 1
rs227959 1.000 0.040 17 3406923 upstream gene variant C/T snv 1
rs4829605 1.000 0.040 X 137182822 intergenic variant C/A;G snv 1
rs640476 1.000 0.040 5 161277998 intergenic variant T/G snv 0.42 1
rs774321998
C1orf167 ; MTHFR
1.000 0.040 1 11790683 missense variant T/C snv 4.0E-06 7.0E-06 1
rs1130399
HLA-DQB1
1.000 0.040 6 32661978 missense variant G/A;T snv 0.20 1
rs9527025
KL
1.000 0.040 13 33054056 missense variant G/C;T snv 0.14 1
rs2534672
MICB
1.000 0.040 6 31497781 intron variant G/C snv 0.32 1
rs10407447
PLD3
1.000 0.040 19 40363275 intron variant A/G snv 0.20 1
rs11667768
PLD3 ; C19orf47
1.000 0.040 19 40348525 5 prime UTR variant C/T snv 6.3E-02 0.11 1
rs11556510
TOMM40
1.000 0.040 19 44891562 missense variant T/G snv 9.8E-03 1.2E-02 1
rs8052688
UBE2I
1.000 0.040 16 1322182 intron variant G/A;C snv 1
rs8063
UBE2I
1.000 0.040 16 1324817 3 prime UTR variant A/C;G snv 4.0E-06; 4.0E-06; 0.71 1
rs4718789 0.925 0.120 7 68579188 intergenic variant C/T snv 8.1E-02 2
rs1451603364
BDNF-AS ; BDNF
0.925 0.120 11 27658411 missense variant C/T snv 4.0E-06 2
rs3756577
CAMK2A
0.925 0.080 5 150249081 intron variant C/T snv 0.14 2
rs3822606
CAMK2A
0.925 0.080 5 150261592 intron variant G/A snv 0.27 2
rs6598008
CDHR5
0.925 0.080 11 618172 intron variant A/G snv 0.48 2
rs4837766
CDK5RAP2
0.925 0.080 9 120402006 intron variant A/C;G;T snv 2
rs111943087
CSF1R
0.925 0.080 5 150059725 missense variant G/A snv 1.4E-05 2
rs9340803
ESR1
0.925 0.080 6 151842832 intron variant A/G snv 1.0E-03 3.8E-04 2
rs35445101
HLA-DRB1
0.925 0.080 6 32579102 missense variant A/G snv 4.2E-04 2.7E-02 2
rs12053868
IL1RAP
0.925 0.080 3 190582215 intron variant A/G snv 8.0E-02 2
rs6850306
LCORL
0.925 0.080 4 18004466 intron variant G/A snv 0.12 2
rs11218304
LOC105369535 ; SORL1
0.925 0.080 11 121478402 intron variant A/G snv 0.30 2