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: rs63750082
rs63750082
13 0.732 0.120 14 73192712 missense variant G/C;T snv 8.0E-06 0.010 1.000 1 2015 2015
dbSNP: rs63750001
rs63750001
4 0.851 0.080 14 73219188 missense variant C/T snv 0.020 1.000 2 2015 2016
dbSNP: rs63750730
rs63750730
6 0.827 0.120 14 73173574 missense variant C/T snv 0.010 1.000 1 2016 2016
dbSNP: rs866914724
rs866914724
3 0.882 0.080 14 73173685 missense variant T/C snv 0.010 1.000 1 2016 2016
dbSNP: rs17125721
rs17125721
14 0.763 0.120 14 73206470 missense variant A/G snv 1.5E-02 1.5E-02 0.050 1.000 5 2000 2017
dbSNP: rs115865530
rs115865530
2 0.925 0.080 14 73206449 missense variant A/G snv 1.4E-04 4.2E-05 0.010 1.000 1 2017 2017
dbSNP: rs63749805
rs63749805
6 0.807 0.120 14 73173577 missense variant C/G;T snv 0.050 1.000 5 1998 2018
dbSNP: rs63750577
rs63750577
8 0.827 0.120 14 73186881 missense variant C/T snv 0.010 1.000 1 2018 2018
dbSNP: rs63750231
rs63750231
23 0.689 0.160 14 73198100 missense variant A/C;G snv 0.100 1.000 14 1996 2019
dbSNP: rs63750526
rs63750526
10 0.776 0.160 14 73192832 missense variant C/A snv 0.100 1.000 10 1997 2019
dbSNP: rs63751037
rs63751037
7 0.790 0.080 14 73173642 missense variant A/G snv 0.020 < 0.001 2 1997 2019
dbSNP: rs201617677
rs201617677
1 1.000 0.080 14 73173698 missense variant G/A;T snv 6.4E-05 0.010 < 0.001 1 2019 2019
dbSNP: rs63749806
rs63749806
7 0.827 0.080 14 73186902 missense variant T/C snv 0.010 < 0.001 1 2019 2019
dbSNP: rs63750299
rs63750299
2 0.925 0.080 14 73186890 missense variant T/G snv 0.010 < 0.001 1 2019 2019
dbSNP: rs63750522
rs63750522
8 0.827 0.120 14 73173644 missense variant G/A;C snv 0.010 < 0.001 1 2019 2019
dbSNP: rs63750900
rs63750900
9 0.763 0.160 14 73198067 missense variant G/A snv 4.0E-06 7.0E-06 0.010 < 0.001 1 2019 2019
dbSNP: rs63750907
rs63750907
6 0.807 0.120 14 73173667 missense variant C/T snv 0.010 < 0.001 1 2019 2019