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: rs387906637
rs387906637
GRIN2A
1 1.000 16 9938314 stop gained G/A snv 0.700 0
dbSNP: rs397518466
rs397518466
GRIN2A
1 1.000 16 10180410 start lost A/G snv 0.700 0
dbSNP: rs397518467
rs397518467
GRIN2A
1 1.000 16 9764715 stop gained G/C snv 0.700 0
dbSNP: rs397518469
rs397518469
GRIN2A
1 1.000 16 9849963 splice acceptor variant T/C snv 0.700 0
dbSNP: rs397518472
rs397518472
GRIN2A
1 1.000 16 9822391 stop gained G/A snv 0.700 0
dbSNP: rs751455326
rs751455326
GRIN2A
2 1.000 16 9768993 missense variant G/A;T snv 4.0E-06 0.700 0
dbSNP: rs761168789
rs761168789
GRIN2A
1 1.000 16 9891000 missense variant G/A snv 4.0E-06 0.700 0
dbSNP: rs796052548
rs796052548
GRIN2A
1 1.000 16 9822378 missense variant A/C snv 0.700 0
dbSNP: rs796052549
rs796052549
GRIN2A ; LOC105371077
2 0.925 0.040 16 9798442 missense variant C/G;T snv 0.700 0
dbSNP: rs796052551
rs796052551
GRIN2A
3 0.882 0.040 16 9768997 missense variant T/C snv 0.700 0
dbSNP: rs869312681
rs869312681
GRIN2A
3 1.000 16 9763169 missense variant T/C snv 0.700 0
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: rs796052543
rs796052543
GRIN2A
1 1.000 16 9840781 missense variant A/G snv 1.5E-05 0.700 0