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: rs140402727
rs140402727
TRIM14 ; NANS
1 1.000 0.280 9 98078196 missense variant G/A;T snv 8.0E-06; 1.3E-04 0.800 1.000 1 2016 2016
dbSNP: rs878852980
rs878852980
TRIM14 ; NANS
1 1.000 0.280 9 98076967 missense variant G/T snv 0.800 1.000 1 2016 2016
dbSNP: rs878852981
rs878852981
TRIM14 ; NANS
1 1.000 0.280 9 98078306 missense variant T/C snv 4.0E-06 3.5E-05 0.800 1.000 1 2016 2016
dbSNP: rs878852982
rs878852982
TRIM14 ; NANS
1 1.000 0.280 9 98080921 missense variant C/T snv 8.0E-06 7.0E-06 0.800 1.000 1 2016 2016
dbSNP: rs1024025721
rs1024025721
TRIM14 ; NANS
1 1.000 0.280 9 98078310 missense variant C/T snv 4.0E-06 1.4E-05 0.700 1.000 1 2016 2016
dbSNP: rs1277263564
rs1277263564
NANS
1 1.000 0.280 9 98056893 missense variant C/A;T snv 4.1E-06 0.700 0
dbSNP: rs779218846
rs779218846
TRIM14 ; NANS
1 1.000 0.280 9 98077018 splice donor variant G/A;T snv 0.700 0
dbSNP: rs878853267
rs878853267
TRIM14 ; NANS
1 1.000 0.280 9 98076953 frameshift variant -/T delins 0.700 0
dbSNP: rs878853268
rs878853268
TRIM14 ; NANS
1 1.000 0.280 9 98082952 inframe insertion -/ATC delins 0.700 0
dbSNP: rs879255602
rs879255602
TRIM14 ; NANS
1 1.000 0.280 9 98078183 frameshift variant GATTAC/ATGG delins 0.700 0