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: rs386833974
rs386833974
CLN5 ; FBXL3
1 1.000 0.120 13 76995980 stop gained C/T snv 0.700 0
dbSNP: rs386833982
rs386833982
CLN5 ; FBXL3
1 1.000 0.120 13 77000663 frameshift variant A/- delins 0.700 0
dbSNP: rs386833983
rs386833983
CLN5 ; FBXL3
1 1.000 0.120 13 77000695 frameshift variant GGAAATGAAACATCTG/- delins 0.700 0
dbSNP: rs730882146
rs730882146
CLN5 ; FBXL3
1 1.000 0.120 13 77000680 missense variant G/A snv 4.0E-06 0.700 0
dbSNP: rs750935331
rs750935331
CLN5 ; FBXL3
1 1.000 0.120 13 77000850 stop gained C/G;T snv 4.1E-06 0.700 0
dbSNP: rs764495616
rs764495616
CLN5 ; FBXL3
1 1.000 0.120 13 77000685 stop gained G/C;T snv 0.700 0
dbSNP: rs764790770
rs764790770
CLN5 ; FBXL3
1 1.000 0.120 13 76992175 stop gained G/A;C snv 2.2E-04 2.8E-05 0.700 0
dbSNP: rs780198002
rs780198002
CLN5 ; FBXL3
1 1.000 0.120 13 76992229 frameshift variant TC/- delins 9.5E-06 0.700 0