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: rs387907129
rs387907129
RHBDF2
1 1.000 0.160 17 76479008 missense variant A/G snv 0.810 1.000 2 2012 2012
dbSNP: rs387907130
rs387907130
RHBDF2
1 1.000 0.160 17 76478999 missense variant G/A snv 0.810 1.000 2 2012 2012