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: rs10488631
rs10488631
13 0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 0.800 1.000 5 2009 2015
dbSNP: rs12531711
rs12531711
5 0.827 0.200 7 128977412 intron variant A/C;G snv 0.800 1.000 1 2011 2011
dbSNP: rs35188261
rs35188261
1 1.000 0.080 7 129043485 intron variant G/A snv 9.0E-02 0.800 1.000 1 2012 2012
dbSNP: rs12539476
rs12539476
1 1.000 0.080 7 129017429 intron variant T/C snv 9.0E-02 0.700 1.000 1 2011 2011
dbSNP: rs13236009
rs13236009
1 1.000 0.080 7 129023119 intron variant T/G snv 9.0E-02 0.700 1.000 1 2012 2012
dbSNP: rs13238352
rs13238352
5 0.827 0.240 7 129007888 intron variant C/T snv 9.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs35234849
rs35234849
1 1.000 0.080 7 129008899 intron variant T/C snv 9.0E-02 0.700 1.000 1 2012 2012