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: rs121434596
rs121434596
18 0.707 0.357 1 114716123 missense variant C/A,G,T snp 4.0E-06; 4.0E-06 0.800 6 1985 2011
dbSNP: rs121913529
rs121913529
70 0.559 0.393 12 25245350 missense variant C/A,G,T snp 4.0E-06 0.700 8 1993 2012
dbSNP: rs112445441
rs112445441
17 0.699 0.286 12 25245347 missense variant snp 0.700 4 1987 2016
dbSNP: rs121913535
rs121913535
9 0.784 0.250 12 25245348 missense variant C/A,G,T snp 0.700 1 2011 2011