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: rs9510787
rs9510787 		1.000 0.120 13 23631056 intron variant A/G snv 0.20
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases 0.730 1.000 4 2010 2018
dbSNP: rs9510787
rs9510787 		1.000 0.120 13 23631056 intron variant A/G snv 0.20
CUI: C0027439
Disease: Nasopharyngeal Neoplasms
Nasopharyngeal Neoplasms 		Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases 0.700 1.000 2 2010 2016
dbSNP: rs11841272
rs11841272 		13 23579314 intron variant T/G snv 0.10
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2019 2019
dbSNP: rs3814787
rs3814787 		13 23578231 intron variant G/C;T snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018