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: rs1883112
rs1883112
3 0.878 0.036 22 36860804 intron variant G/A snp 0.41 0.010 1.000 1 2013 2013
dbSNP: rs28937317
rs28937317
7 0.801 0.107 3 38560418 missense variant T/C snp 0.010 1.000 1 2011 2011
dbSNP: rs58034145
rs58034145
9 0.801 0.143 1 156134830 missense variant A/C snp 0.010 < 0.001 1 2013 2013
dbSNP: rs4673
rs4673
21 0.679 0.429 16 88646828 missense variant A/G,T snp 0.70 0.67 0.010 1.000 1 2013 2013