Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11724839
rs11724839
INTS12 ; GSTCD
2 4 105717099 intron variant T/G snv 5.4E-02 0.700 1.000 1 2010 2010
dbSNP: rs11725523
rs11725523
ARHGEF38
2 4 105596709 intron variant G/A snv 4.4E-02 0.700 1.000 1 2010 2010
dbSNP: rs11726124
rs11726124
INTS12 ; GSTCD
2 4 105845339 intron variant A/G snv 5.5E-02 0.700 1.000 1 2010 2010
dbSNP: rs11726569
rs11726569
ARHGEF38 ; INTS12
2 4 105685451 intron variant A/G snv 5.4E-02 0.700 1.000 1 2010 2010
dbSNP: rs11727348
rs11727348
INTS12 ; GSTCD ; GSTCD-AS1
2 4 105758691 intron variant G/A;T snv 5.4E-02 0.700 1.000 1 2010 2010
dbSNP: rs11727745
rs11727745
INTS12 ; GSTCD ; GSTCD-AS1 ; LOC107986190
2 4 105795370 intron variant T/G snv 5.4E-02 0.700 1.000 1 2010 2010
dbSNP: rs11728044
rs11728044
ARHGEF38 ; INTS12
2 4 105683629 intron variant G/C snv 5.4E-02 0.700 1.000 1 2010 2010
dbSNP: rs11728716
rs11728716
INTS12 ; GSTCD
2 4 105834839 intron variant G/A snv 4.5E-02 0.700 1.000 1 2010 2010
dbSNP: rs11730660
rs11730660
INTS12
2 4 105879222 intron variant A/C snv 4.5E-02 0.700 1.000 1 2010 2010
dbSNP: rs11731417
rs11731417
INTS12 ; GSTCD ; GSTCD-AS1
2 4 105824855 intron variant A/G snv 5.4E-02 0.700 1.000 1 2010 2010
dbSNP: rs11732298
rs11732298
INTS12 ; GSTCD ; GSTCD-AS1
2 4 105780522 intron variant A/T snv 5.4E-02 0.700 1.000 1 2010 2010
dbSNP: rs11732650
rs11732650
INTS12 ; GSTCD
2 4 105833074 intron variant G/A;C snv 0.700 1.000 1 2010 2010
dbSNP: rs11733223
rs11733223
INTS12 ; GSTCD
2 4 105844368 intron variant C/A snv 5.5E-02 0.700 1.000 1 2010 2010
dbSNP: rs11733225
rs11733225
INTS12 ; GSTCD ; GSTCD-AS1
2 4 105784206 intron variant C/G snv 4.4E-02 0.700 1.000 1 2010 2010
dbSNP: rs11733287
rs11733287
INTS12 ; GSTCD ; GSTCD-AS1
2 4 105784182 intron variant G/A snv 5.4E-02 0.700 1.000 1 2010 2010
dbSNP: rs11735213
rs11735213
ARHGEF38
2 4 105606351 intron variant T/G snv 6.2E-02 0.700 1.000 1 2010 2010
dbSNP: rs11735851
rs11735851
INTS12 ; GSTCD ; GSTCD-AS1
2 4 105776097 intron variant G/A snv 4.5E-02 0.700 1.000 1 2010 2010
dbSNP: rs11736859
rs11736859
INTS12 ; GSTCD ; GSTCD-AS1
2 4 105787628 intron variant C/G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs11759653
rs11759653
ADGRG6
2 6 142399217 intron variant G/A snv 0.21 0.700 1.000 1 2010 2010
dbSNP: rs11855326
rs11855326
THSD4
2 15 71318496 intron variant G/A snv 0.31 0.700 1.000 1 2014 2014
dbSNP: rs11858540
rs11858540
THSD4
2 15 71330447 intron variant T/G snv 0.14 0.700 1.000 1 2014 2014
dbSNP: rs12190271
rs12190271
ADGRG6
2 6 142360272 intron variant G/A snv 0.20 0.700 1.000 1 2010 2010
dbSNP: rs12197866
rs12197866
ADGRG6
2 6 142384926 intron variant C/T snv 0.21 0.700 1.000 1 2010 2010
dbSNP: rs12213892
rs12213892
ADGRG6
2 6 142381097 intron variant A/G snv 0.21 0.700 1.000 1 2010 2010
dbSNP: rs12374256
rs12374256
ARHGEF38 ; INTS12
2 4 105696204 intron variant G/A snv 5.4E-02 0.700 1.000 1 2010 2010