Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63750875
MSH2
0.742 0.280 2 47475171 missense variant G/A;C snv 1.6E-05 10
rs1064795747
MSH2
0.925 0.080 2 47412433 missense variant T/C snv 4
rs780178752
MSH2
0.925 0.080 2 47403350 synonymous variant C/T snv 4.3E-06 1.4E-05 2