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: rs1136410
rs1136410
70 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.060 0.667 6 2008 2019
dbSNP: rs1805414
rs1805414
2 0.925 0.080 1 226385663 synonymous variant A/G snv 0.43 0.42 0.030 0.667 3 2007 2018
dbSNP: rs139399785
rs139399785
1 1.000 0.080 1 226380111 stop gained G/A;T snv 4.0E-06; 2.6E-04 0.010 1.000 1 2007 2007
dbSNP: rs1805404
rs1805404
3 0.882 0.200 1 226402257 missense variant G/A;C snv 0.22; 4.0E-06 0.010 < 0.001 1 2013 2013
dbSNP: rs2230484
rs2230484
2 0.925 0.080 1 226383066 missense variant G/A snv 3.7E-03 3.3E-03 0.010 1.000 1 2007 2007
dbSNP: rs3219145
rs3219145
4 0.882 0.120 1 226363128 missense variant T/C;G snv 1.2E-02; 4.0E-06 0.010 1.000 1 2007 2007
dbSNP: rs4653734
rs4653734
2 0.925 0.080 1 226407688 intron variant C/A;G snv 0.010 1.000 1 2019 2019
dbSNP: rs8679
rs8679
7 0.790 0.200 1 226360853 3 prime UTR variant A/G snv 0.16 0.010 1.000 1 2012 2012
dbSNP: rs907187
rs907187
2 0.925 0.080 1 226407946 5 prime UTR variant C/G;T snv 0.21; 4.1E-06 0.010 1.000 1 2019 2019