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: rs190970900
rs190970900 		3 158732213 missense variant T/C snv 5.9E-03 8.5E-03
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs61696028
rs61696028 		3 158737914 non coding transcript exon variant A/C snv 0.18
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs6802315
rs6802315 		0.925 0.040 3 158796571 intron variant T/A snv 0.59
CUI: C0031099
Disease: Periodontitis
Periodontitis 		Stomatognathic Diseases 0.700 1.000 1 2013 2013
dbSNP: rs6802315
rs6802315 		0.925 0.040 3 158796571 intron variant T/A snv 0.59
CUI: C0600298
Disease: Periodontosis
Periodontosis 		Stomatognathic Diseases 0.700 1.000 1 2013 2013
dbSNP: rs7624161
rs7624161 		3 158742125 non coding transcript exon variant C/G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs7635704
rs7635704 		3 158741931 intron variant T/C snv 0.20
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs6441224
rs6441224 		0.925 0.080 3 158732628 intron variant T/C snv 0.58
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2012 2012
dbSNP: rs6441224
rs6441224 		0.925 0.080 3 158732628 intron variant T/C snv 0.58
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2012 2012