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: rs587777041
rs587777041
CYC1
1 1.000 8 144095991 missense variant G/T snv 0.800 1.000 1 2013 2013
dbSNP: rs587777042
rs587777042
CYC1
3 0.882 0.040 8 144096615 missense variant C/T snv 4.0E-06 0.800 1.000 1 2013 2013