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: rs3087456
rs3087456
14 0.742 0.480 16 10877045 intron variant G/A snv 0.53 0.780 0.625 8 2006 2012
dbSNP: rs4774
rs4774
7 0.807 0.240 16 10906991 missense variant G/C snv 0.30 0.28 0.020 0.500 2 2012 2016
dbSNP: rs8048002
rs8048002
4 0.851 0.320 16 10898131 intron variant T/A;C snv 0.010 1.000 1 2012 2012