rs1670661, NELL1

N. diseases: 2
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.
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 1.000 0.040 11 21209124 intron variant C/G;T snv 0.010 1.000 1 2018 2018
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
257 1.000 0.040 11 21209124 intron variant C/G;T snv 0.010 1.000 1 2018 2018