TNXB, tenascin XB, 7148

N. diseases: 127; N. variants: 79
Disease: C4 complement assay (procedure) ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2857009
rs2857009 		1.000 0.080 6 32051969 intron variant G/C snv 0.25
CUI: C0577608
Disease: C4 complement assay (procedure)
C4 complement assay (procedure) 		0.800 1.000 1 2012 2012
dbSNP: rs8283
rs8283 		0.882 0.120 6 32115523 3 prime UTR variant A/G snv 0.25
CUI: C0577608
Disease: C4 complement assay (procedure)
C4 complement assay (procedure) 		0.700 1.000 1 2017 2017