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: rs121913654
rs121913654
3 0.882 0.160 14 23415176 missense variant A/G snv 0.810 1.000 5 2003 2009
dbSNP: rs28933098
rs28933098
4 0.882 0.160 14 23415021 missense variant G/A;T snv 0.810 1.000 4 2003 2007
dbSNP: rs121913649
rs121913649
1 1.000 0.080 14 23413847 missense variant T/A snv 0.800 1.000 4 2003 2007
dbSNP: rs371898076
rs371898076
9 0.763 0.160 14 23426833 missense variant C/T snv 8.0E-06 4.9E-05 0.700 1.000 5 1999 2014
dbSNP: rs121913628
rs121913628
10 0.763 0.160 14 23424059 missense variant C/G;T snv 0.700 0
dbSNP: rs267606908
rs267606908
9 0.763 0.160 14 23424112 missense variant T/C snv 4.0E-06 7.0E-06 0.700 0
dbSNP: rs3218713
rs3218713
10 0.763 0.160 14 23431468 missense variant C/A;T snv 0.700 0
dbSNP: rs3218714
rs3218714
9 0.763 0.160 14 23429279 missense variant G/A;C snv 0.700 0
dbSNP: rs3218716
rs3218716
17 0.716 0.280 14 23425316 missense variant C/A;G;T snv 4.0E-06; 2.4E-05 0.700 0
dbSNP: rs397516127
rs397516127
9 0.763 0.160 14 23426834 missense variant G/A;C snv 0.700 0
dbSNP: rs397516171
rs397516171
9 0.763 0.160 14 23424041 missense variant C/G;T snv 0.700 0
dbSNP: rs397516264
rs397516264
9 0.763 0.160 14 23431602 missense variant C/T snv 4.0E-06 0.700 0
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: rs145734640
rs145734640
3 0.925 0.080 14 23415096 missense variant G/A;C;T snv 1.6E-05; 1.6E-05; 4.0E-06 0.010 1.000 1 2015 2015