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: rs121917837
rs121917837
NEUROG3 ; LOC101929021
1 1.000 0.120 10 69572725 missense variant G/T snv 1.6E-05 1.4E-05 0.800 1.000 1 2006 2006
dbSNP: rs121917838
rs121917838
NEUROG3 ; LOC101929021
1 1.000 0.120 10 69572766 missense variant C/A;T snv 4.0E-06; 4.0E-06 0.800 1.000 1 2006 2006
dbSNP: rs1461650439
rs1461650439
NEUROG3 ; LOC101929021
1 1.000 0.120 10 69572882 stop gained G/T snv 4.2E-06 0.700 0