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: rs9268839
rs9268839
2 0.925 0.160 6 32460995 intron variant A/G snv 0.38 0.710 1.000 2 2012 2013
dbSNP: rs113585425
rs113585425
1 1.000 0.040 6 32465348 intron variant A/C snv 7.8E-02 0.700 1.000 1 2012 2012
dbSNP: rs12525692
rs12525692
1 1.000 0.040 6 32470769 intron variant A/T snv 9.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs12527323
rs12527323
1 1.000 0.040 6 32461917 intron variant C/A snv 9.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs13193827
rs13193827
1 1.000 0.040 6 32462560 intron variant C/A snv 9.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs13217979
rs13217979
1 1.000 0.040 6 32473349 intron variant C/A;T snv 9.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs17202892
rs17202892
1 1.000 0.040 6 32466702 intron variant C/A snv 9.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs28377109
rs28377109
1 1.000 0.040 6 32466939 intron variant C/A snv 9.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs28377518
rs28377518
1 1.000 0.040 6 32464873 intron variant C/T snv 9.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs34200087
rs34200087
1 1.000 0.040 6 32470914 intron variant G/A snv 9.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs35421268
rs35421268
1 1.000 0.040 6 32467419 intron variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs35458464
rs35458464
1 1.000 0.040 6 32463462 intron variant A/G snv 9.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs35954087
rs35954087
1 1.000 0.040 6 32472272 intron variant C/T snv 9.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs372346302
rs372346302
1 1.000 0.040 6 32466946 intron variant -/TA ins 7.0E-06 0.700 1.000 1 2012 2012
dbSNP: rs67209722
rs67209722
1 1.000 0.040 6 32472005 intron variant T/C snv 9.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs72843939
rs72843939
1 1.000 0.040 6 32461300 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs9281838
rs9281838
1 1.000 0.040 6 32466940 intron variant T/-;TT;TTT;TTTT delins 0.29 0.700 1.000 1 2012 2012
dbSNP: rs9791280
rs9791280
1 1.000 0.040 6 32461217 intron variant G/C snv 9.0E-02 0.700 1.000 1 2012 2012