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: rs34557412
rs34557412
TNFRSF13B
15 0.763 0.240 17 16948873 missense variant A/G snv 3.5E-03 3.9E-03 0.800 1.000 1 2005 2005
dbSNP: rs72553882
rs72553882
TNFRSF13B
2 0.925 0.080 17 16940465 stop gained G/C;T snv 4.0E-05 0.700 1.000 1 2009 2009
dbSNP: rs72553883
rs72553883
TNFRSF13B
5 0.851 0.080 17 16940415 missense variant G/A;T snv 2.8E-05; 5.3E-03 0.700 0