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: rs387907340
rs387907340
GNB4
2 0.925 0.080 3 179419444 missense variant C/T snv 0.800 0
dbSNP: rs387907341
rs387907341
GNB4
1 1.000 3 179416495 missense variant T/C snv 0.800 0
dbSNP: rs1553851490
rs1553851490
GNB4
1 1.000 3 179416531 missense variant C/T snv 0.700 0
dbSNP: rs199615251
rs199615251
GNB4
2 0.925 0.080 3 179413452 missense variant T/C snv 4.0E-06 0.700 0