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: rs362691
rs362691
3 0.882 0.120 7 103610714 missense variant G/A;C;T snv 1.2E-05; 0.12 0.010 1.000 1 2013 2013
dbSNP: rs736707
rs736707
6 0.851 0.040 7 103489956 intron variant A/G snv 0.30 0.010 1.000 1 2013 2013
dbSNP: rs73714410
rs73714410
1 1.000 0.040 7 103489775 missense variant C/G;T snv 6.0E-05; 3.1E-03 0.010 1.000 1 2015 2015