PCNX2, pecanex 2, 80003

N. diseases: 11; N. variants: 5
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: rs4649295
rs4649295
0.925 0.080 1 233280792 intron variant T/C snv 0.60
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma
Neoplasms; Endocrine System Diseases 0.700 1.000 1 2017 2017