Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11776675
rs11776675
CDH17
8 94163787 intron variant T/C snv 0.23
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		0.700 1.000 1 2012 2012
dbSNP: rs2514805
rs2514805
CDH17
1.000 0.080 8 94155019 intron variant A/G snv 9.8E-02
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2015 2015
dbSNP: rs1051624
rs1051624
CDH17
1.000 0.080 8 94130944 missense variant T/A;G snv 2.0E-05; 0.51
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.010 1.000 1 2012 2012
dbSNP: rs2243518
rs2243518
CDH17
1.000 0.080 8 94176622 stop gained T/A;C snv 0.77
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.010 1.000 1 2012 2012