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: rs662
rs662
157 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.060 0.833 6 2005 2016
dbSNP: rs3735590
rs3735590
3 0.925 0.080 7 95298183 3 prime UTR variant G/A snv 0.14 0.010 1.000 1 2013 2013
dbSNP: rs705381
rs705381
2 1.000 0.080 7 95324637 upstream gene variant T/C snv 0.72 0.010 < 0.001 1 2013 2013
dbSNP: rs854560
rs854560
113 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1.000 1 2010 2010
dbSNP: rs854571
rs854571
1 7 95325307 upstream gene variant T/C snv 0.62 0.010 1.000 1 2013 2013