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: rs121908047
rs121908047
4 0.851 0.120 1 23798188 missense variant C/T snv 8.0E-06 1.4E-05 0.040 1.000 4 2000 2013
dbSNP: rs137853859
rs137853859
3 0.882 0.120 1 23797718 missense variant G/A;T snv 7.2E-05; 8.0E-06 0.010 1.000 1 2006 2006
dbSNP: rs137853860
rs137853860
3 0.882 0.120 1 23796777 missense variant G/A snv 1.6E-05 7.0E-06 0.010 1.000 1 2006 2006
dbSNP: rs137853861
rs137853861
3 0.882 0.120 1 23796234 missense variant C/T snv 2.0E-05 0.010 1.000 1 2006 2006
dbSNP: rs28940882
rs28940882
3 0.882 0.120 1 23798199 missense variant C/T snv 0.010 1.000 1 2005 2005
dbSNP: rs28940884
rs28940884
3 0.882 0.120 1 23796722 missense variant T/C snv 1.4E-03 5.8E-03 0.010 1.000 1 2005 2005
dbSNP: rs3180383
rs3180383
3 0.882 0.120 1 23796202 missense variant G/A;T snv 0.010 1.000 1 2005 2005
dbSNP: rs368637540
rs368637540
3 0.882 0.120 1 23795992 missense variant C/G;T snv 1.2E-05 0.010 1.000 1 2005 2005