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: rs121917834
rs121917834
9 0.801 0.107 8 22163096 missense variant T/A,C snp 3.6E-05 0.700 4 2004 2009
dbSNP: rs121917835
rs121917835
3 0.878 0.036 8 22164010 missense variant T/A snp 0.700 3 1959 2002
dbSNP: rs121917836
rs121917836
4 0.878 0.036 8 22162727 missense variant G/A snp 0.700 1 2005 2005
dbSNP: rs121918559
rs121918559
1 1.000 0.036 8 22163458 missense variant C/A snp 0.700 1 2005 2005
dbSNP: rs121918560
rs121918560
1 1.000 0.036 8 22164028 missense variant T/C snp 0.700 1 2009 2009
dbSNP: rs34957318
rs34957318
3 0.923 0.071 8 22163947 missense variant G/A snp 1.1E-03 4.7E-03 0.700 1 2004 2004