rs13016963, FLACC1

N. diseases: 5
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.
melanoma
CUI: C0025202
Disease: melanoma
515 0.851 0.080 2 201298088 intron variant A/G snv 0.59 0.800 1.000 2 2011 2017
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.851 0.080 2 201298088 intron variant A/G snv 0.59 0.710 1.000 2 2012 2017
Squamous cell carcinoma of esophagus
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
329 0.851 0.080 2 201298088 intron variant A/G snv 0.59 0.700 1.000 1 2014 2014
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.851 0.080 2 201298088 intron variant A/G snv 0.59 0.010 1.000 1 2017 2017
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.851 0.080 2 201298088 intron variant A/G snv 0.59 0.010 1.000 1 2017 2017