rs12129938, PCNX2

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.
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
145 1.000 0.080 1 233276815 intron variant A/G snv 0.20 0.700 1.000 1 2017 2017