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: rs397514652
rs397514652
1 1.000 15 100887632 missense variant C/T snv 4.0E-06 0.800 1.000 7 2013 2014
dbSNP: rs397514653
rs397514653
1 1.000 15 100914711 missense variant G/A;C snv 8.0E-06 0.800 1.000 7 2013 2014
dbSNP: rs386834230
rs386834230
1 1.000 15 100887578 missense variant G/A snv 7.0E-06 0.700 1.000 7 2013 2014
dbSNP: rs754619607
rs754619607
1 1.000 15 100892598 missense variant C/T snv 4.0E-06 0.700 1.000 7 2013 2014
dbSNP: rs78931658
rs78931658
1 1.000 15 100892640 splice donor variant G/A;C;T snv 4.1E-06 0.700 0