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: rs2073963
rs2073963
7 0.807 0.080 7 18838251 intron variant T/G snv 0.43 0.700 1.000 1 2012 2012
dbSNP: rs71530654
rs71530654
7 0.807 0.080 7 18857365 intron variant A/G snv 0.43 0.700 1.000 1 2017 2017
dbSNP: rs7801037
rs7801037
7 0.807 0.080 7 18857888 intron variant C/A;G;T snv 0.700 1.000 1 2016 2016