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: rs10061804
rs10061804
NPR3
1 5 32748531 intron variant G/A snv 0.30 0.800 1.000 1 2012 2012
dbSNP: rs12213875
rs12213875
LOC101928354
1 6 14586772 intergenic variant A/G snv 0.51 0.800 1.000 1 2012 2012
dbSNP: rs6488619
rs6488619
GRIN2B
1 12 13774962 intron variant C/A;T snv 0.800 1.000 1 2012 2012
dbSNP: rs6543833
rs6543833 		1 2 34405965 intron variant C/A;G snv 0.800 1.000 1 2012 2012