rs2073716, CCHCR1

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 6 31155220 intron variant C/G snv 6.8E-02 0.700 1.000 1 2012 2012