Gene: RRAGD ×
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: rs6907843
rs6907843
RRAGD
2 6 89399655 intron variant C/T snv 0.28 0.700 1.000 1 2018 2018
dbSNP: rs72912510
rs72912510
RRAGD
1 6 89409045 intron variant G/A snv 0.18 0.700 1.000 1 2019 2019