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: rs63751310
rs63751310
6 0.851 0.200 3 37048595 stop gained C/T snv 0.010 1.000 1 2010 2010
dbSNP: rs63751467
rs63751467
2 0.925 0.120 3 37020438 missense variant A/G snv 9.2E-05 5.6E-05 0.010 1.000 1 2018 2018
dbSNP: rs63751612
rs63751612
2 0.925 0.120 3 37047520 missense variant A/G snv 1.2E-04 6.3E-05 0.700 0
dbSNP: rs756045117
rs756045117
3 0.925 0.080 3 37012090 missense variant C/G;T snv 1.6E-05 0.020 1.000 2 2007 2015
dbSNP: rs765480781
rs765480781
1 1.000 0.080 3 37050648 missense variant T/G snv 4.0E-06 0.010 1.000 1 2004 2004
dbSNP: rs876658657
rs876658657
25 0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 0.080 1.000 8 2007 2014
dbSNP: rs876659167
rs876659167
1 1.000 0.080 3 37026001 missense variant A/G snv 0.010 1.000 1 2012 2012