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: rs1473257039
rs1473257039
TNXB
1 1.000 6 32049393 missense variant C/T snv 0.700 0
dbSNP: rs587777683
rs587777683
TNXB
1 1.000 6 32048638 missense variant G/A snv 1.7E-05 0.700 0
dbSNP: rs587777684
rs587777684
TNXB
1 1.000 6 32081419 missense variant C/T snv 7.0E-06 0.700 0