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: rs121913530
rs121913530
39 0.615 0.321 12 25245351 missense variant C/A,G,T snp 0.830 1.000 7 1984 2017
dbSNP: rs121913529
rs121913529
70 0.559 0.393 12 25245350 missense variant C/A,G,T snp 4.0E-06 0.760 1.000 9 2010 2017
dbSNP: rs17851045
rs17851045
20 0.679 0.357 12 25227341 missense variant T/A,G snp 4.0E-06 0.700 2 2004 2006
dbSNP: rs712
rs712
8 0.784 0.107 12 25209618 3 prime UTR variant A/C snp 0.48 0.010 1.000 1 2016 2016