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: rs121918342
rs121918342
1 1.000 0.120 7 138106621 missense variant C/T snv 2.8E-05 1.0E-04 0.800 1.000 4 2003 2010
dbSNP: rs121918343
rs121918343
1 1.000 0.120 7 138091822 missense variant C/T snv 4.0E-06 0.800 1.000 4 2003 2010
dbSNP: rs267606649
rs267606649
1 1.000 0.120 7 138097885 missense variant C/G snv 1.6E-05 3.6E-05 0.800 1.000 4 2003 2010
dbSNP: rs267606650
rs267606650
1 1.000 0.120 7 138107506 missense variant C/T snv 1.2E-05 3.5E-05 0.800 1.000 4 2003 2010
dbSNP: rs1228918719
rs1228918719
1 1.000 0.120 7 138106696 missense variant G/A snv 7.0E-06 0.700 0