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: rs387906956
rs387906956
1 1.000 15 41394999 missense variant T/G snv 0.800 1.000 2 2007 2011
dbSNP: rs387906957
rs387906957
1 1.000 15 41394860 missense variant T/C snv 8.0E-06 7.0E-06 0.800 1.000 2 2007 2011
dbSNP: rs387906958
rs387906958
2 0.925 0.040 15 41394987 missense variant G/A snv 3.2E-05 4.2E-05 0.800 1.000 2 2007 2011
dbSNP: rs376344575
rs376344575
2 0.925 0.040 15 41394885 missense variant C/A;G;T snv 4.0E-06; 4.0E-06; 4.8E-05 0.800 0