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: rs11701
rs11701
2 0.925 0.080 14 20693894 synonymous variant T/A;C;G snv 4.0E-06; 0.14 0.040 0.500 4 2007 2016
dbSNP: rs121909536
rs121909536
5 0.827 0.120 14 20693686 missense variant A/T snv 1.2E-03 9.4E-04 0.030 1.000 3 2009 2019
dbSNP: rs11541242
rs11541242
1 1.000 0.080 14 20693740 missense variant T/C snv 0.020 0.500 2 2012 2014
dbSNP: rs121909539
rs121909539
5 0.827 0.120 14 20693753 missense variant C/G snv 0.010 1.000 1 2019 2019
dbSNP: rs141055235
rs141055235
1 1.000 0.080 14 20693796 missense variant A/G snv 1.7E-04 4.9E-05 0.010 1.000 1 2013 2013
dbSNP: rs17560
rs17560
1 1.000 0.080 14 20693814 missense variant A/G snv 1.4E-03 4.0E-03 0.010 < 0.001 1 2012 2012
dbSNP: rs774017767
rs774017767
1 1.000 0.080 14 20693759 synonymous variant C/T snv 8.0E-06 0.010 < 0.001 1 2012 2012