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: rs199473690
rs199473690
DNMT1
1 1.000 0.080 19 10155017 missense variant T/C snv 0.800 1.000 1 2011 2011
dbSNP: rs199473691
rs199473691
DNMT1
1 1.000 0.080 19 10155029 missense variant GGA/TAT mnv 0.700 0
dbSNP: rs199473692
rs199473692
DNMT1
1 1.000 0.080 19 10155018 missense variant A/G snv 0.700 0