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: rs397518447
rs397518447
GRIN2A
2 0.925 0.040 16 9829585 missense variant G/T snv 0.800 1.000 13 2010 2017
dbSNP: rs397518470
rs397518470
GRIN2A
1 1.000 16 9840745 missense variant C/A;T snv 0.800 1.000 13 2010 2017
dbSNP: rs762659685
rs762659685
GRIN2A
1 1.000 16 9822286 missense variant C/T snv 0.800 1.000 13 2010 2017
dbSNP: rs397514557
rs397514557
GRIN2A
1 1.000 16 9829485 missense variant G/C snv 0.800 1.000 12 2010 2017
dbSNP: rs397518450
rs397518450
GRIN2A
1 1.000 16 9834227 missense variant G/C snv 0.800 1.000 12 2010 2017
dbSNP: rs397518471
rs397518471
GRIN2A
1 1.000 16 9829476 missense variant A/C snv 0.800 1.000 12 2010 2017
dbSNP: rs1250662891
rs1250662891
GRIN2A
2 0.925 0.040 16 10180176 missense variant G/C snv 4.0E-06 0.700 1.000 12 2010 2017
dbSNP: rs1360906241
rs1360906241
GRIN2A
1 1.000 16 9840788 missense variant G/A snv 0.700 1.000 12 2010 2017
dbSNP: rs1555482933
rs1555482933
GRIN2A
2 0.925 0.040 16 9764834 missense variant T/A snv 0.700 1.000 12 2010 2017
dbSNP: rs1555488144
rs1555488144
GRIN2A ; LOC105371077
2 0.925 0.040 16 9798454 missense variant C/T snv 0.700 1.000 12 2010 2017
dbSNP: rs1555491648
rs1555491648
GRIN2A
2 0.925 0.040 16 9822337 missense variant G/A snv 0.700 1.000 12 2010 2017
dbSNP: rs1555496111
rs1555496111
GRIN2A
2 0.925 0.040 16 9849778 missense variant A/G snv 0.700 1.000 12 2010 2017
dbSNP: rs199528312
rs199528312
GRIN2A
1 1.000 16 9938097 missense variant G/A snv 3.6E-05 1.4E-05 0.700 1.000 12 2010 2017
dbSNP: rs397518468
rs397518468
GRIN2A
1 1.000 16 9840706 missense variant G/A snv 0.700 1.000 12 2010 2017
dbSNP: rs886039239
rs886039239
GRIN2A
1 1.000 16 9764617 missense variant T/C snv 8.0E-06 0.700 1.000 12 2010 2017
dbSNP: rs933322445
rs933322445
GRIN2A
1 1.000 16 9764747 missense variant C/T snv 0.700 1.000 12 2010 2017
dbSNP: rs397518465
rs397518465
GRIN2A
2 0.925 0.040 16 9937958 splice donor variant C/A;T snv 0.700 1.000 4 2013 2017
dbSNP: rs1057524089
rs1057524089
GRIN2A
1 1.000 16 9938479 stop gained G/A snv 0.700 0
dbSNP: rs1060503228
rs1060503228
GRIN2A
1 1.000 16 9834148 stop gained G/C snv 0.700 0
dbSNP: rs1064795143
rs1064795143
GRIN2A ; LOC105371077
1 1.000 16 9798269 splice donor variant GGTCTTACCATCACCCACA/- del 0.700 0
dbSNP: rs1445802934
rs1445802934
GRIN2A
1 1.000 16 9822363 missense variant G/A snv 4.0E-06 0.700 0
dbSNP: rs1553340826
rs1553340826
ITSN2
1 1.000 2 24210829 missense variant T/C snv 0.700 0
dbSNP: rs1555483699
rs1555483699
GRIN2A
10 0.851 0.120 16 9768994 missense variant C/T snv 0.700 0
dbSNP: rs1555492758
rs1555492758
GRIN2A
1 1.000 16 9829494 missense variant T/C snv 0.700 0
dbSNP: rs1555492769
rs1555492769
GRIN2A
1 1.000 16 9829529 stop gained C/T snv 0.700 0