CRNN, cornulin, 49860

N. diseases: 22; N. variants: 1
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: rs3829868
rs3829868
0.925 0.080 1 152409644 missense variant C/T snv 0.21 0.15
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma
Digestive System Diseases; Neoplasms 0.700 0