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: rs886039817
rs886039817
GABRB1
1 1.000 4 47403613 missense variant T/C snv 0.800 0
dbSNP: rs886039818
rs886039818
GABRB1
1 1.000 4 47406706 missense variant C/T snv 0.800 0
dbSNP: rs1135401786
rs1135401786
GABRB1
1 1.000 4 47031990 missense variant C/T snv 0.700 0