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: rs104894360
rs104894360
14 0.724 0.560 12 25209904 missense variant T/A;C snv 0.710 1.000 7 2006 2008
dbSNP: rs104894365
rs104894365
3 0.827 0.320 12 25245345 missense variant C/T snv 0.700 1.000 6 2006 2011
dbSNP: rs104894366
rs104894366
9 0.776 0.400 12 25245284 missense variant G/A;C snv 0.700 1.000 4 1993 2011
dbSNP: rs727503108
rs727503108
3 0.882 0.280 12 25227345 missense variant C/A snv 4.0E-06 0.700 1.000 4 2006 2013
dbSNP: rs104894359
rs104894359
4 0.851 0.200 12 25227346 missense variant C/G;T snv 0.700 1.000 3 2006 2011
dbSNP: rs727503109
rs727503109
16 0.752 0.320 12 25245277 missense variant T/C snv 0.700 1.000 3 1993 2009
dbSNP: rs387907205
rs387907205
2 0.925 0.160 12 25227313 missense variant A/C;G snv 0.700 1.000 2 2012 2013
dbSNP: rs397517042
rs397517042
2 0.925 0.200 12 25209896 missense variant A/C;T snv 0.700 1.000 1 2007 2007