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: rs104894603
rs104894603
NOG
1 1.000 0.080 17 56594872 missense variant T/G snv 0.800 1.000 2 1999 2010
dbSNP: rs387906844
rs387906844
NOG
1 1.000 0.080 17 56594919 missense variant C/G;T snv 1.1E-05 0.800 1.000 2 1999 2010
dbSNP: rs104894615
rs104894615
NOG
2 0.925 0.080 17 56594838 missense variant G/C snv 0.700 0
dbSNP: rs1567745119
rs1567745119
NOG
1 1.000 0.080 17 56594837 stop gained G/A snv 0.700 0