Gene: TOP1 ×
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: rs6029526
rs6029526
TOP1
3 20 41043978 intron variant T/A snv 0.58 0.800 1.000 4 2010 2019
dbSNP: rs6065311
rs6065311
TOP1
1 20 41095698 intron variant T/C snv 0.59 0.700 1.000 2 2017 2019