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: rs662
rs662
157 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.100 0.864 22 1996 2018
dbSNP: rs854560
rs854560
113 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.100 0.909 11 2002 2017
dbSNP: rs3735590
rs3735590
3 0.925 0.080 7 95298183 3 prime UTR variant G/A snv 0.14 0.020 1.000 2 2015 2018
dbSNP: rs13306698
rs13306698
3 0.882 0.240 7 95311470 missense variant T/C snv 6.0E-03 1.9E-03 0.010 1.000 1 2003 2003
dbSNP: rs3917481
rs3917481
1 1.000 0.040 7 95321453 intron variant C/T snv 3.7E-02 0.010 1.000 1 2015 2015