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: rs121912981
rs121912981
ALAD
1 1.000 0.160 9 113389085 missense variant C/T snv 3.2E-05 1.4E-05 0.810 1.000 1 2007 2007
dbSNP: rs121912983
rs121912983
ALAD
1 1.000 0.160 9 113389088 missense variant C/T snv 4.0E-06 7.0E-06 0.800 1.000 5 1991 2007
dbSNP: rs121912980
rs121912980
ALAD
1 1.000 0.160 9 113390798 missense variant C/T snv 1.3E-05 4.9E-05 0.800 0
dbSNP: rs121912982
rs121912982
ALAD
1 1.000 0.160 9 113389521 missense variant G/A snv 4.0E-06 1.4E-05 0.700 1.000 5 1991 2007
dbSNP: rs749066913
rs749066913
ALAD
1 1.000 0.160 9 113391634 intron variant G/A;T snv 4.0E-06 0.700 0