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: rs121912575
rs121912575
TNXB
1 1.000 0.160 6 32084536 missense variant C/T snv 8.3E-04 6.7E-04 0.700 1.000 3 2001 2013
dbSNP: rs368512272
rs368512272
TNXB
1 1.000 0.160 6 32098114 missense variant G/A snv 1.6E-05 5.6E-05 0.700 1.000 3 2001 2013
dbSNP: rs587777682
rs587777682
TNXB
2 0.925 0.160 6 32042353 missense variant G/A snv 4.1E-06 0.700 1.000 3 2001 2013