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: rs63750311
rs63750311
8 0.790 0.240 14 73192647 missense variant A/C snv 0.010 1.000 1 2002 2002
dbSNP: rs63750577
rs63750577
8 0.827 0.120 14 73186881 missense variant C/T snv 0.010 1.000 1 2018 2018
dbSNP: rs63750601
rs63750601
3 0.882 0.080 14 73170995 missense variant G/T snv 0.010 1.000 1 1996 1996
dbSNP: rs63750634
rs63750634
3 0.925 0.120 14 73192843 missense variant T/G snv 0.010 1.000 1 2003 2003
dbSNP: rs63750730
rs63750730
6 0.827 0.120 14 73173574 missense variant C/T snv 0.010 1.000 1 2016 2016
dbSNP: rs63750802
rs63750802
7 0.851 0.080 14 73219144 missense variant T/G snv 0.010 1.000 1 2013 2013
dbSNP: rs63750852
rs63750852
8 0.790 0.120 14 73170998 missense variant G/A;T snv 0.010 1.000 1 2006 2006
dbSNP: rs63751032
rs63751032
7 0.851 0.080 14 73219156 missense variant T/A;G snv 0.010 1.000 1 2013 2013
dbSNP: rs63751106
rs63751106
5 0.827 0.080 14 73173643 missense variant T/A;C snv 0.010 1.000 1 2001 2001
dbSNP: rs63751141
rs63751141
3 0.882 0.080 14 73170984 missense variant G/C snv 0.010 1.000 1 2000 2000
dbSNP: rs63751163
rs63751163
7 0.807 0.120 14 73192844 missense variant T/C snv 0.010 1.000 1 1998 1998
dbSNP: rs63751235
rs63751235
6 0.807 0.120 14 73198117 missense variant C/G snv 0.010 1.000 1 2000 2000
dbSNP: rs63751420
rs63751420
2 0.925 0.080 14 73198040 missense variant C/T snv 0.010 1.000 1 1996 1996
dbSNP: rs63751441
rs63751441
3 0.882 0.080 14 73173684 missense variant C/G;T snv 5.2E-05 0.010 1.000 1 2001 2001
dbSNP: rs661
rs661
6 0.807 0.120 14 73217225 missense variant G/A;T snv 4.0E-06 0.010 1.000 1 2006 2006
dbSNP: rs779296437
rs779296437
2 0.925 0.080 14 73192699 missense variant A/T snv 4.0E-06 0.010 1.000 1 2011 2011
dbSNP: rs866914724
rs866914724
3 0.882 0.080 14 73173685 missense variant T/C snv 0.010 1.000 1 2016 2016