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: rs104893959
rs104893959
GCM2
2 0.925 0.040 6 10877343 missense variant C/A;T snv 2.0E-05; 8.0E-06 0.010 1.000 1 2006 2006