Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2071295
rs2071295
TNXB
0.925 0.120 6 32070923 intron variant C/T snv 0.25
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 3 2007 2011
dbSNP: rs2071295
rs2071295
TNXB
0.925 0.120 6 32070923 intron variant C/T snv 0.25
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		0.700 1.000 1 2010 2010