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: rs35576928
rs35576928
PRM1 ; RMI2 ; LOC105371082
1 1.000 0.040 16 11281137 missense variant C/A;G snv 8.7E-03; 4.0E-06 0.010 1.000 1 2012 2012