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: rs121434569
rs121434569
29 0.667 0.321 7 55181378 missense variant C/T snp 2.8E-05 9.6E-05 0.020 1.000 2 2009 2014
dbSNP: rs1045642
rs1045642
108 0.520 0.714 7 87509329 synonymous variant A/G,T snp 0.50 0.56 0.010 1.000 1 2006 2006
dbSNP: rs113488022
rs113488022
267 0.407 0.786 7 140753336 missense variant snp 4.0E-06 0.010 1.000 1 2014 2014
dbSNP: rs121434568
rs121434568
33 0.642 0.321 7 55191822 missense variant T/A,G snp 0.010 1.000 1 2014 2014
dbSNP: rs121913459
rs121913459
16 0.707 0.143 9 130872896 missense variant C/T snp 0.010 1.000 1 2006 2006
dbSNP: rs121913488
rs121913488
7 0.821 0.107 13 28018505 stop gained C/A,G,T snp 0.010 1.000 1 2012 2012
dbSNP: rs748843032
rs748843032
5 0.846 0.107 4 99594840 missense variant T/C snp 4.0E-06 0.010 1.000 1 2006 2006