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: rs11638416
rs11638416
1 15 58598915 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs16940571
rs16940571
1 15 58590593 3 prime UTR variant C/T snv 3.5E-02 0.700 1.000 1 2012 2012
dbSNP: rs17269425
rs17269425
1 15 58639141 intron variant A/G snv 2.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs347118
rs347118
1 15 58708424 intron variant G/A snv 3.5E-02 0.700 1.000 1 2012 2012
dbSNP: rs347122
rs347122
1 15 58747033 intron variant T/C snv 3.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs387005
rs387005
1 15 58717866 intron variant T/C snv 3.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs424346
rs424346
1 15 58718763 intron variant C/T snv 3.5E-02 0.700 1.000 1 2012 2012
dbSNP: rs437549
rs437549
1 15 58731360 intron variant T/A snv 3.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs602921
rs602921
1 15 58711735 intron variant C/T snv 3.5E-02 0.700 1.000 1 2012 2012
dbSNP: rs793417
rs793417
1 15 58703238 intron variant T/C snv 3.6E-02 0.700 1.000 1 2012 2012