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: rs8027714
rs8027714 		1.000 0.040 15 24719450 intron variant G/A snv 0.11
CUI: C0877015
Disease: Pelvic Organ Prolapse
Pelvic Organ Prolapse 		Pathological Conditions, Signs and Symptoms 0.710 1.000 2 2011 2018
dbSNP: rs4467035
rs4467035 		15 24343404 non coding transcript exon variant G/T snv 0.34
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2019 2019
dbSNP: rs772577429
rs772577429 		1.000 0.080 15 24675977 missense variant G/A;C snv 1.4E-05; 1.8E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.700 0
dbSNP: rs778802437
rs778802437 		1.000 0.080 15 24676207 missense variant G/A;T snv 5.4E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.700 0