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: rs397509391
rs397509391
DNMT1
1 1.000 19 10154602 missense variant C/A snv 0.820 1.000 2 2012 2019
dbSNP: rs397509393
rs397509393
DNMT1
1 1.000 19 10154604 missense variant C/G;T snv 0.810 1.000 2 2012 2019
dbSNP: rs397509392
rs397509392
DNMT1
1 1.000 19 10154709 missense variant G/A;C snv 0.810 1.000 1 2012 2012