Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10747478 1.000 0.040 1 96435899 intergenic variant T/A;C;G snv 1
rs1285957 1.000 0.040 7 141889478 downstream gene variant T/C snv 0.86 1
rs13100344 1.000 0.040 3 94886263 intergenic variant T/A snv 0.40 1
rs145241704 1.000 0.040 7 141805287 upstream gene variant T/G snv 7.4E-02 1
rs370838138 1.000 0.040 5 25081736 intergenic variant G/C snv 0.42 1
rs56156506 1.000 0.040 X 38140399 intron variant A/T snv 0.33 1
rs62090893 1.000 0.040 18 75338379 intergenic variant G/A snv 9.7E-02 1
rs7532266 1.000 0.040 1 23225130 regulatory region variant A/C snv 0.66 1
rs6589488
CADM1
1.000 0.040 11 115226236 intron variant A/T snv 0.90 1
rs6590474
CNTN5
1.000 0.040 11 99982441 intron variant A/C snv 0.71 1
rs737582
CNTN5
1.000 0.040 11 99992669 intron variant G/A snv 0.39 1
rs7947224
CNTN5
1.000 0.040 11 100002678 intron variant T/C snv 0.39 1
rs923768
CSGALNACT1
1.000 0.040 8 19673452 intron variant T/C snv 0.46 1
rs2287348
ERLEC1 ; GPR75-ASB3 ; ASB3
1.000 0.040 2 53812676 intron variant C/A;T snv 1
rs726281
ESR1
1.000 0.040 6 151981443 intron variant G/A snv 0.56 1
rs1298806501
ESR2
1.000 0.040 14 64227600 missense variant G/A snv 4.0E-06 1
rs9874207
FOXP1
1.000 0.040 3 70970599 non coding transcript exon variant T/C snv 0.64 1
rs752298108
GHRL ; GHRLOS
1.000 0.040 3 10286806 missense variant C/T snv 4.0E-05 7.0E-06 1
rs3749073
GPR55
1.000 0.040 2 230910379 missense variant C/A snv 0.12 0.17 1
rs10096097
LEPROTL1 ; DCTN6
1.000 0.040 8 30169582 intron variant G/A snv 0.62 1
rs117957029
LOC105370064
1.000 0.040 12 127200688 intron variant T/C snv 1.4E-02 1
rs200312312
LOC105379109
1.000 0.040 5 104666645 intron variant T/C snv 0.16 1
rs2008387
MGMT
1.000 0.040 10 129650500 intron variant G/A snv 0.36 1
rs9821797
NCKIPSD
1.000 0.040 3 48680820 intron variant T/A snv 0.20 1
rs778902328
NPY ; LOC107986777
1.000 0.040 7 24291679 missense variant A/G snv 4.0E-06 7.0E-06 1