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: rs63750206
rs63750206
9 0.807 0.200 3 36996701 missense variant G/A;C;T snv 0.720 0.947 19 1995 2014
dbSNP: rs63750217
rs63750217
10 0.807 0.240 3 37048955 missense variant G/A;C snv 0.720 1.000 15 1975 2017
dbSNP: rs587778966
rs587778966
3 0.925 0.160 3 36996698 frameshift variant -/C delins 0.720 0.500 2 2006 2009
dbSNP: rs63750781
rs63750781
6 0.851 0.160 3 37004444 missense variant C/G;T snv 4.0E-06 0.710 1.000 39 1996 2013
dbSNP: rs63751194
rs63751194
7 0.851 0.160 3 37017508 missense variant C/A;T snv 4.0E-06 0.710 1.000 25 1999 2014
dbSNP: rs587778914
rs587778914
2 0.925 0.160 3 36996645 missense variant A/C snv 0.710 1.000 1 2012 2012
dbSNP: rs587778937
rs587778937
4 0.882 0.160 3 37040291 missense variant T/C;G snv 0.710 1.000 1 2013 2013
dbSNP: rs63749818
rs63749818
2 0.925 0.160 3 37007002 stop gained C/A;G;T snv 0.710 1.000 1 2012 2012
dbSNP: rs63749939
rs63749939
6 0.851 0.160 3 36996702 missense variant G/A snv 0.710 < 0.001 1 2009 2009
dbSNP: rs63750211
rs63750211
5 0.882 0.160 3 37008904 missense variant A/G snv 0.710 1.000 1 2012 2012
dbSNP: rs63750693
rs63750693
3 0.882 0.160 3 37047652 missense variant T/A;C snv 0.710 1.000 1 2010 2010
dbSNP: rs63750710
rs63750710
3 0.925 0.160 3 37020411 missense variant A/C snv 0.710 1.000 1 1997 1997
dbSNP: rs63750899
rs63750899
7 0.851 0.200 3 37048562 missense variant C/G;T snv 0.710 1.000 1 2004 2004
dbSNP: rs63751608
rs63751608
3 0.925 0.160 3 37042321 missense variant T/C snv 0.710 1.000 1 2005 2005
dbSNP: rs63751247
rs63751247
5 0.882 0.200 3 37047632 inframe deletion AAG/- delins 0.700 1.000 16 1997 2018
dbSNP: rs63749795
rs63749795
8 0.807 0.240 3 37028833 stop gained C/T snv 0.700 1.000 14 1992 2016
dbSNP: rs63751275
rs63751275
6 0.851 0.240 3 37048973 missense variant C/A;G;T snv 1.2E-05; 2.0E-05 0.700 1.000 13 2002 2017
dbSNP: rs63751711
rs63751711
4 0.925 0.160 3 37012099 missense variant G/A;T snv 0.700 1.000 13 1996 2016
dbSNP: rs63749909
rs63749909
4 0.925 0.160 3 37028891 missense variant T/A;C snv 7.0E-06 0.700 1.000 12 1996 2015
dbSNP: rs63750792
rs63750792
4 0.925 0.160 3 36993630 missense variant C/T snv 0.700 1.000 12 1999 2013
dbSNP: rs63750453
rs63750453
5 0.882 0.160 3 37001051 missense variant G/A snv 0.700 1.000 11 2001 2015
dbSNP: rs63750437
rs63750437
4 0.925 0.160 3 37000977 missense variant G/A;C snv 0.700 1.000 10 1997 2014
dbSNP: rs63750641
rs63750641
2 0.925 0.160 3 37000997 missense variant A/G snv 0.700 1.000 10 1999 2010
dbSNP: rs267607789
rs267607789
3 1.000 0.160 3 37014545 splice donor variant G/A;C;T snv 0.700 1.000 9 1996 2016
dbSNP: rs63749906
rs63749906
2 0.925 0.160 3 36993651 missense variant T/G snv 0.700 1.000 8 1995 2007