Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6855246 1.000 0.040 4 102191313 intergenic variant A/G snv 0.14 4
rs35225200 1.000 0.040 4 102225731 intergenic variant A/C snv 5.4E-02 5
rs1409313
CUEDC2
1.000 0.040 10 102431844 intron variant T/C snv 0.85 2
rs7907645 1.000 0.040 10 102664043 downstream gene variant T/G snv 0.13 2
rs11191419
BORCS7-ASMT ; BORCS7
1.000 0.040 10 102852578 intron variant T/A snv 0.36 2
rs11191454
LOC107984265 ; BORCS7-ASMT ; AS3MT
0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 9
rs7914558
CNNM2
0.851 0.040 10 103016151 intron variant G/A snv 0.40 5
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 13
rs11191582
NT5C2
1.000 0.040 10 103153896 intron variant G/A snv 7.7E-02 2
rs10149470 1.000 0.040 14 103551616 upstream gene variant A/G snv 0.54 3
rs12887734
COA8 ; KLC1
1.000 0.040 14 103580497 intron variant G/T snv 0.26 2
rs9879311
ATP2B2
1.000 0.040 3 10373659 intron variant C/A;T snv 2
rs17292804
PPP1R13B
1.000 0.040 14 103738786 synonymous variant G/A snv 8.0E-02 8.5E-02 2
rs8009147
PPP1R13B
1.000 0.040 14 103798325 intron variant A/G;T snv 2
rs11185408 1 104249635 intergenic variant G/A;C snv 0.55 1
rs325506
LOC105379109
1.000 0.040 5 104676602 intron variant C/G;T snv 2
rs61867293
SORCS3
1.000 0.040 10 104804166 intron variant C/T snv 0.15 2
rs111931861
KMT2E
7 105103772 non coding transcript exon variant A/G snv 4.5E-02 1
rs9297357
ZFPM2 ; LOC105375695
0.851 0.040 8 105130105 intron variant C/G;T snv 5
rs41563
SRPK2
1.000 0.040 7 105212207 intron variant G/A;C snv 2
rs4580973
SRPK2
1.000 0.040 7 105263212 intron variant A/G snv 0.45 2
rs10099100 8 10719265 downstream gene variant G/C snv 0.32 3
rs12871532 0.851 0.040 13 108016199 intergenic variant T/C snv 0.46 5
rs4773054 1.000 0.040 13 109501681 intron variant T/C snv 0.89 2
rs427691 1.000 0.040 5 109678809 intergenic variant G/A snv 0.23 2