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: rs1051168
rs1051168
NMB
2 1.000 0.080 15 84657289 missense variant G/C;T snv 4.5E-06; 0.22 0.010 1.000 1 2011 2011