Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10005067 4 87931491 intergenic variant T/A;C snv 1
rs10037512
MEF2C-AS1
5 89058858 intron variant T/A;C snv 3
rs10048146 1.000 0.040 16 86677054 regulatory region variant A/G snv 0.17 3
rs10048745
ARHGAP25
2 68735005 5 prime UTR variant G/A snv 0.24 2
rs1007738
CKAP5
11 46827809 intron variant G/A snv 0.64 1
rs10085588
LOC105375412 ; SEM1 ; LOC105375411
1.000 0.080 7 96508362 intron variant A/G snv 0.72 3
rs10086835
COLEC10
8 119027942 intron variant C/T snv 0.63 1
rs10091277
COLEC10
8 119022148 intron variant A/G snv 0.53 1
rs10098408
COLEC10
8 119027482 intron variant T/C snv 0.58 1
rs10101385 8 118911611 regulatory region variant A/G snv 0.34 1
rs10120794 9 130550694 intergenic variant G/A snv 0.40 1
rs1021188 13 42541997 intergenic variant C/T snv 0.79 2
rs10226308
EPDR1 ; NME8
7 37898820 intron variant A/C;G snv 2
rs1023940
LOC107986528 ; CCDC170
6 151611643 intron variant A/G snv 0.58 1
rs10242100 7 121343289 downstream gene variant A/G snv 0.29 2
rs1036066
GNG12-AS1 ; WLS
1 68194522 intron variant A/C snv 0.33 1
rs1037011 12 106909000 upstream gene variant T/C snv 0.64 1
rs1038304
CCDC170 ; LOC107986528
0.882 0.160 6 151612040 intron variant A/G snv 0.58 4
rs10416218
GPATCH1
19 33108221 intron variant T/C snv 0.42 2
rs10429035
SEM1 ; LOC105375411
7 96490169 intron variant G/A snv 0.39 2
rs10450586 11 27286936 intergenic variant G/C snv 0.60 1
rs10457487
RSPO3 ; LOC112267972
6 127198089 3 prime UTR variant C/A snv 0.42 1
rs10464592
SEM1
7 96601374 intron variant G/A snv 0.34 1
rs10490046
SLC8A1
2 40403538 intron variant A/C snv 0.28 1
rs10493013 1 22376542 regulatory region variant T/C snv 0.20 1