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: rs12742923
rs12742923
1 1.000 0.160 1 83024161 intron variant C/T snv 0.13 0.700 1.000 1 2012 2012
dbSNP: rs17154929
rs17154929
1 1.000 0.160 10 44029227 intergenic variant C/T snv 2.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs404005
rs404005
1 1.000 0.160 2 40168938 intron variant C/T snv 0.59 0.700 1.000 1 2012 2012
dbSNP: rs7996217
rs7996217
1 1.000 0.160 13 101348594 intron variant T/G snv 1.6E-02 0.700 1.000 1 2012 2012