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: rs2812393
rs2812393
6 0.807 0.080 1 231777927 intron variant G/C snv 0.61 0.010 1.000 1 2012 2012
dbSNP: rs766288
rs766288
7 0.790 0.080 1 231557942 intron variant G/T snv 0.40 0.010 1.000 1 2012 2012
dbSNP: rs821616
rs821616
13 0.752 0.200 1 232008852 missense variant A/T snv 0.26 0.29 0.010 1.000 1 2012 2012