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: rs121908827
rs121908827
1 1.000 0.040 2 96254107 missense variant A/G snv 0.800 1.000 5 2010 2014
dbSNP: rs121908828
rs121908828
1 1.000 0.040 2 96254106 missense variant C/A;T snv 4.0E-06 0.800 1.000 5 2010 2014
dbSNP: rs121908818
rs121908818
1 0.925 0.080 2 96265224 stop gained C/G;T snv 7.0E-06 0.700 1.000 2 2010 2010
dbSNP: rs121908819
rs121908819
1 1.000 0.040 2 96265174 missense variant C/T snv 2.0E-04 7.2E-04 0.700 1.000 2 2010 2010
dbSNP: rs121908820
rs121908820
1 1.000 0.040 2 96265165 missense variant C/G snv 3.7E-05 3.5E-05 0.700 1.000 2 2010 2010
dbSNP: rs121908823
rs121908823
1 1.000 0.040 2 96254974 missense variant C/T snv 6.7E-04 2.6E-03 0.700 1.000 2 2010 2010
dbSNP: rs121908824
rs121908824
1 1.000 0.040 2 96254962 missense variant G/A;C;T snv 2.0E-05; 4.0E-06 0.700 1.000 2 2010 2010