Gene: MSH2 ×
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: rs63750875
rs63750875
MSH2
15 0.742 0.280 2 47475171 missense variant G/A;C snv 1.6E-05 0.030 1.000 3 2004 2008
dbSNP: rs1064795747
rs1064795747
MSH2
4 0.925 0.080 2 47412433 missense variant T/C snv 0.010 1.000 1 2010 2010
dbSNP: rs780178752
rs780178752
MSH2
2 0.925 0.080 2 47403350 synonymous variant C/T snv 4.3E-06 1.4E-05 0.010 1.000 1 2007 2007