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: rs768119894
rs768119894
1 1.000 7 103636370 missense variant T/C snv 1.6E-05 0.800 1.000 1 2015 2015
dbSNP: rs201044262
rs201044262
1 1.000 7 103640597 missense variant G/A;C snv 1.6E-04 0.700 1.000 1 2015 2015
dbSNP: rs794727996
rs794727996
1 1.000 7 103635498 missense variant G/T snv 0.700 0
dbSNP: rs794727997
rs794727997
1 1.000 7 103503158 missense variant C/A;T snv 4.0E-06 0.700 0
dbSNP: rs794727998
rs794727998
1 1.000 7 103636250 missense variant T/C snv 0.700 0
dbSNP: rs794727999
rs794727999
1 1.000 7 103490747 missense variant C/T snv 0.700 0
dbSNP: rs797045000
rs797045000
1 1.000 7 103630111 missense variant G/A snv 0.700 0