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: rs1800546
rs1800546
1 1.000 0.080 9 101427574 missense variant C/G snv 3.0E-03 3.1E-03 0.700 1.000 16 1983 2017
dbSNP: rs137854523
rs137854523
4 0.851 0.240 11 22236206 missense variant G/T snv 1.0E-03 9.6E-04 0.700 1.000 7 2010 2015
dbSNP: rs76917243
rs76917243
1 1.000 0.080 9 101427498 missense variant G/T snv 3.6E-04 3.0E-04 0.700 1.000 10 1990 2015
dbSNP: rs145078268
rs145078268
1 1.000 0.080 9 101424931 missense variant C/G;T snv 4.0E-06; 2.1E-04 0.700 1.000 3 2000 2013
dbSNP: rs77718928
rs77718928
1 1.000 0.080 9 101421891 missense variant G/A;C snv 1.5E-04; 3.2E-05 0.700 1.000 7 1998 2015
dbSNP: rs78340951
rs78340951
1 1.000 0.080 9 101421899 missense variant G/A;C snv 4.0E-06; 1.2E-04 0.800 1.000 19 1988 2012
dbSNP: rs118204429
rs118204429
1 1.000 0.080 9 101429901 stop gained G/A;T snv 8.4E-05; 1.2E-05 0.700 1.000 7 1994 2015
dbSNP: rs41281039
rs41281039
1 1.000 0.080 9 101429943 missense variant T/A snv 4.4E-05 1.4E-05 0.010 1.000 1 2010 2010
dbSNP: rs752902486
rs752902486
1 1.000 0.080 9 101427500 stop gained G/A;C snv 3.6E-05 2.8E-05 0.700 1.000 1 2006 2006
dbSNP: rs118204430
rs118204430
1 1.000 0.080 9 101427580 missense variant A/C;G snv 4.0E-06; 2.8E-05 0.700 0
dbSNP: rs900220679
rs900220679
1 1.000 0.080 9 101421809 stop lost C/G snv 2.0E-05 7.0E-06 0.700 0
dbSNP: rs199965465
rs199965465
1 1.000 0.080 9 101425044 splice acceptor variant T/G snv 1.6E-05 0.700 0
dbSNP: rs555935217
rs555935217
1 1.000 0.080 9 101424932 missense variant G/A snv 1.2E-05 2.1E-05 0.700 1.000 11 1988 2010
dbSNP: rs138121153
rs138121153
1 1.000 0.080 9 101428468 splice donor variant C/A;T snv 1.2E-05 0.700 0
dbSNP: rs764826805
rs764826805
1 1.000 0.080 9 101429754 splice donor variant C/T snv 4.0E-06 0.700 1.000 1 2015 2015
dbSNP: rs750026492
rs750026492
1 1.000 0.080 9 101429755 splice region variant C/T snv 4.0E-06 0.700 1.000 4 2002 2010
dbSNP: rs369586696
rs369586696
1 1.000 0.080 9 101421877 missense variant A/G snv 4.0E-06 2.1E-05 0.710 1.000 11 1988 2010
dbSNP: rs786204598
rs786204598
1 1.000 0.080 9 101429964 splice acceptor variant CCTA/- delins 4.0E-06 2.8E-05 0.700 1.000 1 1990 1990
dbSNP: rs1057517421
rs1057517421
1 1.000 0.080 9 101427602 frameshift variant T/- delins 4.0E-06 0.700 0
dbSNP: rs864309533
rs864309533
1 1.000 0.080 9 101424977 frameshift variant G/- delins 4.0E-06 7.0E-06 0.700 1.000 1 2005 2005
dbSNP: rs1172384674
rs1172384674
1 1.000 0.080 9 101424878 stop gained C/A;T snv 4.0E-06; 4.0E-06 0.700 0
dbSNP: rs118204428
rs118204428
1 1.000 0.080 9 101430878 stop gained G/A snv 4.0E-06 0.700 1.000 7 1994 2010
dbSNP: rs764701775
rs764701775
1 1.000 0.080 9 101425482 missense variant A/G snv 4.0E-06 0.700 1.000 11 1988 2010
dbSNP: rs781023784
rs781023784
1 1.000 0.080 9 101429858 missense variant A/G snv 4.0E-06 0.700 1.000 11 1988 2010
dbSNP: rs387906225
rs387906225
1 1.000 0.080 9 101428485 frameshift variant TGTT/- delins 7.0E-05 0.700 1.000 12 1990 2015