Gene: FBXO11 ×
Source: INFERRED ×
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: rs63749843
rs63749843
MSH6 ; FBXO11
7 0.827 0.240 2 47803449 stop gained C/A;G;T snv 0.700 1.000 12 2002 2018
dbSNP: rs63750741
rs63750741
MSH6 ; FBXO11
4 0.827 0.200 2 47799329 missense variant T/C snv 1.2E-05 0.710 1.000 2 2004 2005
dbSNP: rs587779287
rs587779287
MSH6 ; FBXO11
1 0.827 0.200 2 47806280 frameshift variant GTACATTATTTTC/- delins 0.700 0
dbSNP: rs63750138
rs63750138
MSH6 ; FBXO11
3 0.851 0.160 2 47800297 missense variant C/A;G;T snv 2.0E-05; 8.0E-06 0.720 1.000 13 2001 2019
dbSNP: rs63750617
rs63750617
MSH6 ; FBXO11
5 0.851 0.160 2 47803473 missense variant C/G;T snv 4.0E-06; 9.5E-05 0.700 1.000 12 2006 2017
dbSNP: rs63751017
rs63751017
MSH6 ; FBXO11
6 0.851 0.240 2 47800714 stop gained C/A;T snv 1.4E-05 0.700 1.000 12 2003 2017
dbSNP: rs63750258
rs63750258
MSH6 ; FBXO11
2 0.851 0.200 2 47800966 stop gained G/A;C;T snv 0.700 1.000 8 2001 2015
dbSNP: rs267608058
rs267608058
MSH6 ; FBXO11
6 0.851 0.200 2 47800130 frameshift variant TCAG/- delins 7.0E-06 0.700 1.000 5 1999 2012
dbSNP: rs63749999
rs63749999
MSH6 ; FBXO11
6 0.851 0.240 2 47801086 stop gained C/T snv 1.2E-05 0.700 0
dbSNP: rs267608078
rs267608078
MSH6 ; FBXO11
5 0.882 0.160 2 47803501 frameshift variant C/-;CC;CCC delins 0.700 1.000 33 1997 2017
dbSNP: rs63751127
rs63751127
MSH6 ; FBXO11
3 0.882 0.200 2 47800177 stop gained C/A;T snv 4.0E-06; 4.0E-06 0.700 1.000 7 2004 2017
dbSNP: rs63749873
rs63749873
MSH6 ; FBXO11
5 0.882 0.160 2 47795903 stop gained C/G snv 4.0E-06 1.4E-05 0.700 1.000 6 1999 2018
dbSNP: rs1021631442
rs1021631442
MSH6 ; FBXO11
3 0.882 0.200 2 47806279 missense variant G/A snv 0.700 1.000 1 2012 2012
dbSNP: rs1553413710
rs1553413710
MSH6 ; FBXO11
3 0.882 0.200 2 47800325 missense variant C/T snv 0.700 1.000 1 2013 2013
dbSNP: rs267608059
rs267608059
MSH6 ; FBXO11
5 0.882 0.240 2 47801050 stop gained G/T snv 0.700 0
dbSNP: rs63750111
rs63750111
MSH6 ; FBXO11
3 0.882 0.200 2 47800914 stop gained C/A;G snv 0.700 0
dbSNP: rs864622607
rs864622607
MSH6 ; FBXO11
3 0.882 0.200 2 47803678 missense variant T/G snv 0.700 0
dbSNP: rs869312769
rs869312769
MSH6 ; FBXO11
5 0.882 0.160 2 47799334 frameshift variant T/- delins 0.700 0
dbSNP: rs267608094
rs267608094
MSH6 ; FBXO11
4 0.925 0.160 2 47806641 stop gained C/A;T snv 4.1E-06; 4.1E-06 0.700 1.000 11 2005 2016
dbSNP: rs267608120
rs267608120
MSH6 ; FBXO11
4 0.925 0.160 2 47806606 frameshift variant CAAG/- delins 0.700 1.000 8 2003 2015
dbSNP: rs63751327
rs63751327
MSH6 ; FBXO11
4 0.925 0.160 2 47804984 frameshift variant -/A;AA delins 0.700 1.000 8 1999 2010
dbSNP: rs587779227
rs587779227
MSH6 ; FBXO11
4 0.925 0.160 2 47800040 missense variant G/A snv 1.4E-05 0.700 1.000 7 2008 2017
dbSNP: rs63750767
rs63750767
MSH6 ; FBXO11
4 0.925 0.160 2 47806588 stop gained -/TCAAAAGGGACATAGAAAA delins 7.0E-06 0.700 1.000 7 2003 2016
dbSNP: rs63750955
rs63750955
MSH6 ; FBXO11
4 0.925 0.160 2 47798633 frameshift variant -/T delins 1.4E-05 0.700 1.000 6 2000 2010
dbSNP: rs267608098
rs267608098
MSH6 ; FBXO11
4 0.925 0.160 2 47804908 splice acceptor variant A/G;T snv 0.700 1.000 5 1999 2015