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: rs3218716
rs3218716
17 0.716 0.280 14 23425316 missense variant C/A;G;T snv 4.0E-06; 2.4E-05 0.800 1.000 32 1975 2017
dbSNP: rs3218713
rs3218713
10 0.763 0.160 14 23431468 missense variant C/A;T snv 0.800 1.000 42 1991 2017
dbSNP: rs371898076
rs371898076
9 0.763 0.160 14 23426833 missense variant C/T snv 8.0E-06 4.9E-05 0.800 1.000 39 1992 2017
dbSNP: rs121913628
rs121913628
10 0.763 0.160 14 23424059 missense variant C/G;T snv 0.800 1.000 34 1992 2017
dbSNP: rs3218714
rs3218714
9 0.763 0.160 14 23429279 missense variant G/A;C snv 0.800 1.000 30 1992 2017
dbSNP: rs267606908
rs267606908
9 0.763 0.160 14 23424112 missense variant T/C snv 4.0E-06 7.0E-06 0.800 1.000 27 1992 2017
dbSNP: rs397516171
rs397516171
9 0.763 0.160 14 23424041 missense variant C/G;T snv 0.800 1.000 25 1992 2017
dbSNP: rs397516127
rs397516127
9 0.763 0.160 14 23426834 missense variant G/A;C snv 0.800 1.000 20 1992 2005
dbSNP: rs397516264
rs397516264
9 0.763 0.160 14 23431602 missense variant C/T snv 4.0E-06 0.700 1.000 2 2007 2009
dbSNP: rs267606910
rs267606910
6 0.807 0.080 14 23431589 missense variant C/T snv 8.0E-06 0.800 1.000 26 1992 2017
dbSNP: rs727504753
rs727504753
6 0.807 0.160 14 23429345 missense variant C/T snv 0.700 0
dbSNP: rs863224900
rs863224900
6 0.807 0.160 14 23428534 missense variant A/C;G;T snv 0.700 0
dbSNP: rs121913624
rs121913624
4 0.851 0.080 14 23429278 missense variant C/A;G;T snv 0.800 1.000 76 1961 2017
dbSNP: rs36211715
rs36211715
5 0.851 0.080 14 23424839 missense variant C/A;G;T snv 4.0E-06 0.800 1.000 39 1992 2017
dbSNP: rs121913630
rs121913630
7 0.851 0.080 14 23425814 missense variant G/A;C snv 1.2E-05 0.800 1.000 35 1992 2017
dbSNP: rs121913625
rs121913625
4 0.851 0.080 14 23429005 missense variant G/A;C;T snv 0.800 1.000 34 1990 2014
dbSNP: rs121913627
rs121913627
8 0.851 0.080 14 23427657 missense variant C/A;G;T snv 4.0E-06 0.800 1.000 30 1992 2014
dbSNP: rs121913638
rs121913638
4 0.851 0.120 14 23425980 missense variant C/T snv 0.800 1.000 22 1992 2005
dbSNP: rs727503260
rs727503260
4 0.851 0.080 14 23425403 missense variant C/G;T snv 0.800 1.000 14 2003 2017
dbSNP: rs1566535410
rs1566535410
5 0.851 0.080 14 23429297 missense variant T/C snv 0.700 0
dbSNP: rs730880750
rs730880750
4 0.851 0.080 14 23424843 missense variant G/A;C;T snv 0.700 0
dbSNP: rs121913637
rs121913637
3 0.882 0.080 14 23425971 missense variant G/A snv 7.0E-06 0.800 1.000 50 1992 2017
dbSNP: rs121913631
rs121913631
3 0.882 0.080 14 23424107 missense variant G/C snv 1.4E-05 0.800 1.000 37 1992 2017
dbSNP: rs397516209
rs397516209
3 0.882 0.080 14 23432713 missense variant C/T snv 4.0E-06 7.0E-06 0.800 1.000 36 1992 2017
dbSNP: rs121913641
rs121913641
3 0.882 0.080 14 23425970 missense variant C/G;T snv 0.800 1.000 35 1992 2017