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: rs11100860
rs11100860
LOC105377462
4 4 144557987 intron variant A/G snv 0.43 0.700 1.000 2 2009 2010
dbSNP: rs11134779
rs11134779
ADAM19
2 5 157509758 intron variant A/G snv 0.42 0.700 1.000 1 2010 2010
dbSNP: rs11155242
rs11155242
ADGRG6
2 6 142370412 missense variant A/C snv 0.19 0.20 0.700 1.000 1 2010 2010
dbSNP: rs11168048
rs11168048
HTR4 ; LOC107986462
4 5 148462790 intron variant T/C snv 0.38 0.700 1.000 1 2010 2010
dbSNP: rs11168049
rs11168049
HTR4 ; LOC107986462
2 5 148475701 intron variant T/C snv 0.37 0.700 1.000 1 2010 2010
dbSNP: rs11172113
rs11172113
LRP1
10 0.882 0.080 12 57133500 intron variant T/C snv 0.42 0.700 1.000 1 2011 2011
dbSNP: rs11257613
rs11257613
CDC123
2 10 12242393 intron variant G/A;C snv 0.700 1.000 1 2010 2010
dbSNP: rs113096699
rs113096699
ADGRG6
2 6 142424746 intron variant -/G ins 0.700 1.000 1 2010 2010
dbSNP: rs11598305
rs11598305
CDC123
2 10 12227401 intron variant C/A;G snv 0.700 1.000 1 2010 2010
dbSNP: rs11722225
rs11722225
INTS12 ; GSTCD
5 4 105845273 intron variant T/C snv 5.5E-02 0.700 1.000 1 2010 2010
dbSNP: rs11723225
rs11723225
INTS12 ; GSTCD ; GSTCD-AS1
2 4 105824908 intron variant C/T snv 5.4E-02 0.700 1.000 1 2010 2010
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: rs11727189
rs11727189
ARHGEF38 ; INTS12
4 4 105697983 intron variant G/T 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: rs11727735
rs11727735
INTS12 ; GSTCD
3 1.000 0.040 4 105710713 intron variant A/G snv 4.4E-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