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: rs7574865
rs7574865
59 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.810 1.000 3 2012 2014
dbSNP: rs3024921
rs3024921
2 0.925 0.120 2 191078546 intron variant A/T snv 3.6E-02 0.800 1.000 2 2012 2012
dbSNP: rs10168266
rs10168266
8 0.776 0.400 2 191071078 intron variant C/T snv 0.19 0.710 1.000 2 2014 2017
dbSNP: rs10181656
rs10181656
9 0.763 0.360 2 191105153 intron variant G/C snv 0.79 0.010 1.000 1 2014 2014
dbSNP: rs11889341
rs11889341
12 0.732 0.480 2 191079016 intron variant C/T snv 0.21 0.010 1.000 1 2014 2014
dbSNP: rs8179673
rs8179673
3 0.882 0.240 2 191104615 intron variant C/G;T snv 0.010 1.000 1 2014 2014