Gene: MSH6 ×
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: rs267608078
rs267608078
MSH6 ; FBXO11
5 0.882 0.160 2 47803501 frameshift variant C/-;CC;CCC delins 0.700 1.000 16 1997 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 13 2003 2017
dbSNP: rs63751327
rs63751327
MSH6 ; FBXO11
4 0.925 0.160 2 47804984 frameshift variant -/A;AA delins 0.700 1.000 12 1999 2017
dbSNP: rs267608120
rs267608120
MSH6 ; FBXO11
4 0.925 0.160 2 47806606 frameshift variant CAAG/- delins 0.700 1.000 9 2003 2014
dbSNP: rs267608092
rs267608092
MSH6 ; FBXO11
4 0.925 0.160 2 47803553 frameshift variant TT/-;T;TTT delins 0.700 1.000 8 2002 2016
dbSNP: rs267608121
rs267608121
MSH6 ; FBXO11
4 0.925 0.160 2 47806630 frameshift variant -/GTCA delins 0.700 1.000 8 2003 2016
dbSNP: rs587779227
rs587779227
MSH6 ; FBXO11
4 0.925 0.160 2 47800040 missense variant G/A snv 1.4E-05 0.700 1.000 8 2008 2017
dbSNP: rs587779279
rs587779279
MSH6 ; FBXO11
3 1.000 0.160 2 47806203 splice acceptor variant G/A snv 0.700 1.000 7 2009 2016
dbSNP: rs267608122
rs267608122
MSH6 ; FBXO11
4 0.925 0.160 2 47806651 missense variant G/A;C snv 0.700 1.000 6 1999 2016
dbSNP: rs63749942
rs63749942
MSH6 ; FBXO11
3 1.000 0.160 2 47806279 inframe deletion CGT/- delins 0.700 1.000 6 2007 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 1999 2010
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: rs587782386
rs587782386
MSH6 ; FBXO11
1 2 47800909 missense variant C/T snv 7.0E-06 0.700 1.000 5 2002 2015
dbSNP: rs63750647
rs63750647
MSH6 ; FBXO11
1 2 47800283 inframe deletion CCT/- delins 0.700 1.000 5 2007 2014
dbSNP: rs63750854
rs63750854
MSH6 ; FBXO11
3 1.000 0.160 2 47799402 frameshift variant -/TG delins 0.700 1.000 5 2002 2013
dbSNP: rs63750949
rs63750949
MSH6 ; FBXO11
6 0.827 0.080 2 47806213 missense variant C/A;T snv 0.700 1.000 5 2002 2013
dbSNP: rs63751113
rs63751113
MSH6 ; FBXO11
2 1.000 0.080 2 47800910 missense variant G/A snv 0.700 1.000 5 2002 2015
dbSNP: rs1553408388
rs1553408388
MSH6
2 2 47783453 stop gained G/T snv 0.700 1.000 4 2006 2015
dbSNP: rs267608042
rs267608042
MSH6 ; FBXO11
3 1.000 0.160 2 47801101 frameshift variant TT/- delins 0.700 1.000 4 2007 2017
dbSNP: rs267608050
rs267608050
MSH6 ; FBXO11
2 1.000 0.160 2 47799764 frameshift variant T/- delins 0.700 1.000 4 1999 2012
dbSNP: rs267608076
rs267608076
MSH6 ; FBXO11
3 1.000 0.160 2 47799618 frameshift variant AG/- delins 0.700 1.000 4 2006 2016
dbSNP: rs587779204
rs587779204
MSH6 ; FBXO11
3 1.000 0.160 2 47799092 missense variant T/C snv 0.700 1.000 4 2013 2017
dbSNP: rs587779220
rs587779220
MSH6 ; FBXO11
1 2 47799737 missense variant T/C snv 0.700 1.000 4 2007 2015
dbSNP: rs587779263
rs587779263
MSH6 ; FBXO11
3 1.000 0.160 2 47804909 splice acceptor variant G/T snv 0.700 1.000 4 2010 2015
dbSNP: rs63749843
rs63749843
MSH6 ; FBXO11
7 0.827 0.240 2 47803449 stop gained C/A;G;T snv 0.700 1.000 4 2002 2014