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: rs154774636
rs154774636
1 1.000 0.107 15 68229568 missense variant C/G snp 0.800 2 1988 2011
dbSNP: rs154774633
rs154774633
1 1.000 0.107 15 68214387 missense variant A/G snp 0.800 1 2011 2011
dbSNP: rs154774634
rs154774634
1 1.000 0.107 15 68211853 missense variant C/T snp 1.6E-05 0.800 1 2011 2011
dbSNP: rs154774635
rs154774635
1 1.000 0.107 15 68218595 missense variant G/A snp 0.800 1 2011 2011
dbSNP: rs154774638
rs154774638
1 1.000 0.107 15 68211715 missense variant C/T snp 3.2E-05 3.2E-05 0.700 1 2011 2011
dbSNP: rs154774641
rs154774641
1 1.000 0.107 15 68214356 missense variant G/C,T snp 0.700 1 2011 2011
dbSNP: rs387907043
rs387907043
3 0.923 0.107 20 63930873 missense variant T/A,G snp 4.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs63750391
rs63750391
5 0.821 0.214 14 73173665 missense variant G/A,T snp 0.010 1.000 1 2011 2011