Source: ALL
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: rs121964920
rs121964920
C7
2 0.925 0.080 5 40959520 missense variant C/A;T snv 2.3E-03; 1.6E-05 0.800 1.000 3 1996 1998
dbSNP: rs121964921
rs121964921
C7
2 1.000 0.080 5 40955428 missense variant G/A;C;T snv 1.6E-05; 1.3E-04; 5.3E-05 0.800 1.000 3 1996 1998
dbSNP: rs541873000
rs541873000
C7
1 1.000 0.080 5 40972564 missense variant G/C snv 0.700 1.000 3 1996 1998
dbSNP: rs531103546
rs531103546
C7
1 1.000 0.080 5 40936337 splice acceptor variant G/T snv 1.2E-04 1.4E-05 0.700 1.000 1 2005 2005
dbSNP: rs113187203
rs113187203
C7
1 1.000 0.080 5 40972580 missense variant G/A;T snv 3.9E-04; 2.1E-05 0.700 0
dbSNP: rs121964922
rs121964922
C7
1 1.000 0.080 5 40958230 stop gained T/A snv 0.700 0
dbSNP: rs369349760
rs369349760
C7
1 1.000 0.080 5 40945289 missense variant G/A snv 1.4E-04 1.7E-04 0.700 0
dbSNP: rs387906509
rs387906509
C7
1 1.000 0.080 5 40979743 stop gained T/A snv 0.700 0