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: rs1047266
rs1047266
TNFRSF10B
1 1.000 0.080 8 23043188 missense variant G/A;T snv 9.7E-02; 8.0E-06 0.010 1.000 1 2009 2009