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: rs4149584
rs4149584
TNFRSF1A
24 0.683 0.440 12 6333477 missense variant C/G;T snv 4.0E-06; 1.3E-02 0.010 1.000 1 2011 2011
dbSNP: rs750667928
rs750667928
IL12RB1
2 0.925 0.120 19 18077542 missense variant G/A snv 8.1E-06 0.010 1.000 1 2017 2017