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: rs4273077
rs4273077
TNFRSF13B
4 0.925 0.160 17 16945825 intron variant A/G snv 0.13 0.810 1.000 2 2013 2014