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: rs730880030
rs730880030
CHCHD10 ; LOC107985577
4 0.851 0.080 22 23767591 missense variant C/A snv 0.700 1.000 9 2014 2018
dbSNP: rs587777574
rs587777574
CHCHD10 ; LOC107985577
4 0.882 0.040 22 23767459 missense variant G/A snv 0.700 1.000 1 2014 2014