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: rs11209026
rs11209026
46 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.900 0.773 22 2006 2020
dbSNP: rs7517847
rs7517847
19 0.689 0.600 1 67215986 intron variant T/G snv 0.37 0.720 1.000 3 2006 2010
dbSNP: rs11581607
rs11581607
4 0.925 0.040 1 67242007 intron variant G/A snv 4.6E-02 0.700 1.000 1 2017 2017
dbSNP: rs1004819
rs1004819
9 0.776 0.360 1 67204530 intron variant G/A snv 0.30 0.020 1.000 2 2007 2012
dbSNP: rs10889677
rs10889677
40 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 0.010 1.000 1 2020 2020
dbSNP: rs11465797
rs11465797
2 1.000 0.040 1 67200769 missense variant C/A snv 0.010 1.000 1 2016 2016
dbSNP: rs376377228
rs376377228
3 0.925 0.040 1 67182950 missense variant A/G snv 1.6E-05 2.1E-05 0.010 < 0.001 1 2008 2008
dbSNP: rs41313262
rs41313262
3 0.925 0.040 1 67240217 missense variant G/A;T snv 1.1E-02 1.0E-02 0.010 < 0.001 1 2016 2016
dbSNP: rs7530511
rs7530511
12 0.742 0.400 1 67219704 missense variant T/A;C snv 0.88 0.010 1.000 1 2010 2010
dbSNP: rs758102857
rs758102857
3 0.925 0.040 1 67206957 missense variant A/G snv 4.0E-06 0.010 1.000 1 2009 2009