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: rs730882155
rs730882155
NARS2
1 1.000 11 78528890 missense variant G/A snv 1.6E-05 2.8E-05 0.800 0
dbSNP: rs1565216037
rs1565216037
NARS2
1 1.000 11 78465898 missense variant T/C snv 0.700 1.000 1 2015 2015
dbSNP: rs565224393
rs565224393
NARS2
3 0.882 0.200 11 78469304 stop gained A/C;G;T snv 4.0E-06; 4.0E-06 0.700 1.000 1 2015 2015
dbSNP: rs1035101172
rs1035101172
NARS2
1 1.000 11 78559538 splice donor variant C/A;G;T snv 4.0E-06; 4.0E-06 0.700 0
dbSNP: rs1565235204
rs1565235204
NARS2 ; LOC105369403
1 1.000 11 78493178 missense variant A/C snv 0.700 0
dbSNP: rs201751992
rs201751992
NARS2
1 1.000 11 78571419 missense variant T/C;G snv 2.4E-05; 8.0E-06 0.700 0
dbSNP: rs367584549
rs367584549
NARS2
1 1.000 11 78571435 missense variant G/A snv 5.6E-05 2.1E-05 0.700 0
dbSNP: rs730882154
rs730882154
NARS2 ; LOC105369403
1 1.000 11 78493063 missense variant C/G snv 0.700 0
dbSNP: rs750594551
rs750594551
NARS2
1 1.000 11 78566145 missense variant T/C snv 8.1E-06 7.0E-06 0.700 0
dbSNP: rs755122704
rs755122704
NARS2
1 1.000 11 78528900 missense variant A/T snv 8.0E-06 7.0E-06 0.700 0
dbSNP: rs763770414
rs763770414
NARS2
1 1.000 11 78443739 missense variant A/C;G snv 1.2E-05 7.0E-06 0.700 0