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: rs11809491
rs11809491
2 1 65954975 intron variant G/T snv 2.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs17128817
rs17128817
2 1 66346417 intron variant C/T snv 2.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs486438
rs486438
2 1 66208980 intron variant A/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs567279
rs567279
4 1 66222346 intron variant G/T snv 0.97 0.700 1.000 1 2012 2012