Gene: RFC1 ×
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: rs6835111
rs6835111
RFC1
2 4 39359449 intron variant A/G snv 0.37 0.700 1.000 1 2018 2018
dbSNP: rs6844176
rs6844176
RFC1
1 4 39364970 intron variant T/C snv 0.37 0.700 1.000 1 2019 2019
dbSNP: rs78773383
rs78773383
RFC1
2 4 39364100 intron variant A/G snv 0.49 0.700 1.000 1 2016 2016