Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7085104
BORCS7-ASMT ; AS3MT
1.000 0.040 10 102869116 intron variant A/G snv 0.35 2
rs12764899
AS3MT ; BORCS7-ASMT
1.000 0.040 10 102875346 intron variant G/A snv 0.21 4
rs12244388
BORCS7-ASMT ; AS3MT
1.000 0.040 10 102880295 intron variant G/A;T snv 1
rs10883795
AS3MT ; BORCS7-ASMT
1.000 0.040 10 102894820 intron variant T/C snv 0.30 1
rs11191454
LOC107984265 ; BORCS7-ASMT ; AS3MT
0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 5
rs7897654
LOC107984265
1.000 0.040 10 102902701 intron variant T/C snv 0.30 1
rs11722779
SLC9B1
1.000 0.040 4 102906331 3 prime UTR variant T/G snv 0.58 1
rs4129148 1.000 0.040 Y 1029445 intergenic variant C/G;T snv 1
rs55833108
CNNM2
1.000 0.040 10 102981826 intron variant G/T snv 0.14 1
rs7914558
CNNM2
0.851 0.040 10 103016151 intron variant G/A snv 0.40 5
rs10786736
CNNM2 ; NT5C2
1.000 0.040 10 103089359 3 prime UTR variant G/C snv 9.9E-02 1
rs10883832
NT5C2
1.000 0.040 10 103111522 intron variant T/G snv 8.4E-02 1
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 10
rs11191582
NT5C2
1.000 0.040 10 103153896 intron variant G/A snv 7.7E-02 2
rs12416331
NT5C2
1.000 0.040 10 103169157 intron variant T/A snv 8.4E-02 2
rs10860964
C12orf42
1.000 0.040 12 103202677 intergenic variant T/C snv 0.28 1
rs190474885 1.000 0.040 10 103213560 upstream gene variant C/T snv 1.7E-02 1
rs9554958 1.000 0.040 13 103448176 upstream gene variant A/G snv 0.52 1
rs35559831 1.000 0.040 2 103486682 intergenic variant G/A;C snv 2
rs4906335 0.925 0.040 14 103554804 intron variant C/A;G snv 2
rs11597473
NEURL1
1.000 0.040 10 103559284 intron variant G/C;T snv 1
rs12887734
COA8 ; KLC1
1.000 0.040 14 103580497 intron variant G/T snv 0.26 2
rs35229468
KLC1 ; COA8
1.000 0.040 14 103585720 intron variant C/T snv 0.25 2
rs10895475 1.000 0.040 11 103593113 intergenic variant C/A;T snv 1
rs9879311
ATP2B2
1.000 0.040 3 10373659 intron variant C/A;T snv 2