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: rs63750252
rs63750252
MSH6 ; FBXO11
1 1.000 0.160 2 47804959 missense variant A/G;T snv 1.0E-03 0.700 1.000 9 1997 2012