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: rs4331881
rs4331881
ADAM19
2 5 157517467 intron variant G/T snv 0.42 0.700 1.000 2 2010 2010
dbSNP: rs6889822
rs6889822
HTR4 ; LOC107986462
2 5 148467144 intron variant A/G snv 0.34 0.700 1.000 2 2010 2010
dbSNP: rs10050159
rs10050159
INTS12 ; GSTCD
2 4 105844758 intron variant G/A snv 0.11 0.700 1.000 1 2010 2010
dbSNP: rs10050333
rs10050333
INTS12 ; GSTCD
2 4 105844656 intron variant T/A snv 0.11 0.700 1.000 1 2010 2010
dbSNP: rs10078178
rs10078178
ADAM19
2 5 157505976 intron variant A/T snv 0.42 0.700 1.000 1 2010 2010
dbSNP: rs1040525
rs1040525
ADGRG6
2 6 142382532 intron variant C/A;G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs1040526
rs1040526
ADGRG6
2 6 142414679 intron variant A/G snv 0.40 0.700 1.000 1 2010 2010
dbSNP: rs10463406
rs10463406
HTR4 ; LOC107986462
2 5 148459281 intron variant C/A;T snv 0.700 1.000 1 2010 2010
dbSNP: rs10484733
rs10484733
ADGRG6
2 6 142389851 intron variant C/G snv 0.21 0.700 1.000 1 2010 2010
dbSNP: rs10498230
rs10498230
LINC01807
2 2 228637787 intron variant C/T snv 7.3E-02 0.700 1.000 1 2010 2010
dbSNP: rs10512249
rs10512249
PTCH1
2 9 95494027 intron variant G/A snv 0.11 0.700 1.000 1 2010 2010
dbSNP: rs10516525
rs10516525
INTS12 ; GSTCD ; GSTCD-AS1
2 4 105746868 intron variant T/C snv 4.4E-02 0.700 1.000 1 2010 2010
dbSNP: rs10516527
rs10516527
INTS12 ; GSTCD ; GSTCD-AS1
2 4 105813189 intron variant A/G snv 5.4E-02 0.700 1.000 1 2010 2010
dbSNP: rs10516529
rs10516529
INTS12
2 4 105878159 intron variant T/G snv 0.12 0.700 1.000 1 2010 2010
dbSNP: rs10824425
rs10824425 		2 10 76580552 intergenic variant G/C snv 0.42 0.700 1.000 1 2014 2014
dbSNP: rs10922530
rs10922530
KYAT3
2 1 88961569 intron variant G/A snv 0.31 0.700 1.000 1 2007 2007
dbSNP: rs11067283
rs11067283
LOC107984437
2 12 114758086 intron variant T/A snv 0.24 0.700 1.000 1 2010 2010
dbSNP: rs11097901
rs11097901
INTS12 ; GSTCD ; GSTCD-AS1
2 4 105808776 intron variant C/T snv 5.9E-02 0.700 1.000 1 2010 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: rs11168049
rs11168049
HTR4 ; LOC107986462
2 5 148475701 intron variant T/C snv 0.37 0.700 1.000 1 2010 2010
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: rs11723225
rs11723225
INTS12 ; GSTCD ; GSTCD-AS1
2 4 105824908 intron variant C/T snv 5.4E-02 0.700 1.000 1 2010 2010