rs17006292, TFCP2L1

N. diseases: 1
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 1.000 0.200 2 121261187 intron variant C/A snv 2.8E-02 0.800 1.000 1 2012 2012