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: rs11662308
rs11662308 		18 21585516 intron variant T/G snv 0.15
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement 		0.700 1.000 1 2018 2018
dbSNP: rs12373434
rs12373434 		18 21532778 intron variant T/C;G snv
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement 		0.700 1.000 1 2018 2018
dbSNP: rs973730
rs973730 		18 21573533 synonymous variant C/T snv 0.84 0.83
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement 		0.700 1.000 1 2018 2018
dbSNP: rs35087820
rs35087820 		0.925 0.080 18 21574272 missense variant T/C snv 2.0E-02 1.9E-02
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2009 2009
dbSNP: rs35087820
rs35087820 		0.925 0.080 18 21574272 missense variant T/C snv 2.0E-02 1.9E-02
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2009 2009