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: rs4785763
rs4785763 		0.925 0.120 16 90000528 non coding transcript exon variant A/C;T snv
CUI: C0025202
Disease: melanoma
melanoma 		Neoplasms 0.800 1.000 2 2009 2017
dbSNP: rs4238833
rs4238833 		1.000 0.040 16 89984281 intron variant G/T snv 0.60
CUI: C0025202
Disease: melanoma
melanoma 		Neoplasms 0.700 1.000 2 2011 2012
dbSNP: rs10584116
rs10584116 		16 89995916 non coding transcript exon variant CT/- delins 0.14
CUI: C0424621
Disease: Body Fat Distribution
Body Fat Distribution 		0.700 1.000 1 2019 2019
dbSNP: rs11076650
rs11076650 		1.000 0.040 16 90001533 non coding transcript exon variant G/A snv 0.49
CUI: C0025202
Disease: melanoma
melanoma 		Neoplasms 0.700 1.000 1 2011 2011
dbSNP: rs11648898
rs11648898 		1.000 0.040 16 89979578 non coding transcript exon variant A/G snv 0.17
CUI: C0025202
Disease: melanoma
melanoma 		Neoplasms 0.700 1.000 1 2011 2011
dbSNP: rs11649211
rs11649211 		16 89973042 intron variant G/C snv 0.64
CUI: C0406208
Disease: Suntan
Suntan 		0.700 1.000 1 2018 2018
dbSNP: rs35176381
rs35176381 		16 89996071 non coding transcript exon variant G/A;C snv
CUI: C0406208
Disease: Suntan
Suntan 		0.700 1.000 1 2018 2018
dbSNP: rs4238833
rs4238833 		1.000 0.040 16 89984281 intron variant G/T snv 0.60
CUI: C0018498
Disease: Hair Color
Hair Color 		0.700 1.000 1 2008 2008
dbSNP: rs4408545
rs4408545 		1.000 0.040 16 89977620 non coding transcript exon variant C/G;T snv 0.40
CUI: C0018498
Disease: Hair Color
Hair Color 		0.700 1.000 1 2008 2008
dbSNP: rs4408545
rs4408545 		1.000 0.040 16 89977620 non coding transcript exon variant C/G;T snv 0.40
CUI: C0025202
Disease: melanoma
melanoma 		Neoplasms 0.700 1.000 1 2011 2011
dbSNP: rs4785759
rs4785759 		1.000 0.040 16 89984472 intron variant A/C;G snv
CUI: C0025202
Disease: melanoma
melanoma 		Neoplasms 0.700 1.000 1 2011 2011
dbSNP: rs4785763
rs4785763 		0.925 0.120 16 90000528 non coding transcript exon variant A/C;T snv
CUI: C0018498
Disease: Hair Color
Hair Color 		0.700 1.000 1 2008 2008
dbSNP: rs4785763
rs4785763 		0.925 0.120 16 90000528 non coding transcript exon variant A/C;T snv
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases 0.700 1.000 1 2010 2010
dbSNP: rs575866787
rs575866787 		16 89986579 intron variant G/A snv 1.1E-02
CUI: C0018498
Disease: Hair Color
Hair Color 		0.700 1.000 1 2018 2018
dbSNP: rs8063160
rs8063160 		16 89988301 intron variant T/C;G snv
CUI: C0018498
Disease: Hair Color
Hair Color 		0.700 1.000 1 2015 2015