NCOA6, nuclear receptor coactivator 6, 23054

N. diseases: 64; N. variants: 36
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: rs4911442
rs4911442 		1.000 0.040 20 34767243 intron variant G/A snv 0.93
CUI: C0025202
Disease: melanoma
melanoma 		Neoplasms 0.720 1.000 3 2008 2014
dbSNP: rs1018503
rs1018503 		20 34737712 intron variant T/A;G snv
CUI: C1168438
Disease: Protein C antigen measurement
Protein C antigen measurement 		0.700 1.000 1 2010 2010
dbSNP: rs1018503
rs1018503 		20 34737712 intron variant T/A;G snv
CUI: C0919677
Disease: Protein C measurement
Protein C measurement 		0.700 1.000 1 2010 2010
dbSNP: rs13040449
rs13040449 		20 34771098 intron variant T/A snv 0.31
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs13044899
rs13044899 		20 34699274 intron variant G/A snv 0.41
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2017 2017
dbSNP: rs13044899
rs13044899 		20 34699274 intron variant G/A snv 0.41
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		Cardiovascular Diseases 0.700 1.000 1 2019 2019
dbSNP: rs144057587
rs144057587 		20 34770790 intron variant C/T snv 1.1E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs1998028
rs1998028 		20 34756792 intron variant A/T snv 0.34
CUI: C1168438
Disease: Protein C antigen measurement
Protein C antigen measurement 		0.700 1.000 1 2010 2010
dbSNP: rs1998028
rs1998028 		20 34756792 intron variant A/T snv 0.34
CUI: C0919677
Disease: Protein C measurement
Protein C measurement 		0.700 1.000 1 2010 2010
dbSNP: rs2180276
rs2180276 		20 34772982 intron variant T/A snv 0.35
CUI: C0919677
Disease: Protein C measurement
Protein C measurement 		0.700 1.000 1 2010 2010
dbSNP: rs2180276
rs2180276 		20 34772982 intron variant T/A snv 0.35
CUI: C1168438
Disease: Protein C antigen measurement
Protein C antigen measurement 		0.700 1.000 1 2010 2010
dbSNP: rs2295353
rs2295353 		20 34768708 intron variant C/T snv 0.33
CUI: C0919677
Disease: Protein C measurement
Protein C measurement 		0.700 1.000 1 2010 2010
dbSNP: rs2295353
rs2295353 		20 34768708 intron variant C/T snv 0.33
CUI: C1168438
Disease: Protein C antigen measurement
Protein C antigen measurement 		0.700 1.000 1 2010 2010
dbSNP: rs2378259
rs2378259 		20 34753885 intron variant G/A snv 0.48
CUI: C1168438
Disease: Protein C antigen measurement
Protein C antigen measurement 		0.700 1.000 1 2010 2010
dbSNP: rs2378259
rs2378259 		20 34753885 intron variant G/A snv 0.48
CUI: C0919677
Disease: Protein C measurement
Protein C measurement 		0.700 1.000 1 2010 2010
dbSNP: rs2424997
rs2424997 		20 34797002 intron variant A/G;T snv
CUI: C1168438
Disease: Protein C antigen measurement
Protein C antigen measurement 		0.700 1.000 1 2010 2010
dbSNP: rs2424997
rs2424997 		20 34797002 intron variant A/G;T snv
CUI: C0919677
Disease: Protein C measurement
Protein C measurement 		0.700 1.000 1 2010 2010
dbSNP: rs2425001
rs2425001 		20 34807065 intron variant A/G;T snv
CUI: C1168438
Disease: Protein C antigen measurement
Protein C antigen measurement 		0.700 1.000 1 2010 2010
dbSNP: rs2425001
rs2425001 		20 34807065 intron variant A/G;T snv
CUI: C0919677
Disease: Protein C measurement
Protein C measurement 		0.700 1.000 1 2010 2010
dbSNP: rs3787222
rs3787222 		20 34745236 intron variant T/A snv 0.34
CUI: C0919677
Disease: Protein C measurement
Protein C measurement 		0.700 1.000 1 2010 2010
dbSNP: rs3787222
rs3787222 		20 34745236 intron variant T/A snv 0.34
CUI: C1168438
Disease: Protein C antigen measurement
Protein C antigen measurement 		0.700 1.000 1 2010 2010
dbSNP: rs4911441
rs4911441 		20 34728742 intron variant T/A;C snv
CUI: C1168438
Disease: Protein C antigen measurement
Protein C antigen measurement 		0.700 1.000 1 2010 2010
dbSNP: rs4911441
rs4911441 		20 34728742 intron variant T/A;C snv
CUI: C0919677
Disease: Protein C measurement
Protein C measurement 		0.700 1.000 1 2010 2010
dbSNP: rs4911442
rs4911442 		1.000 0.040 20 34767243 intron variant G/A snv 0.93
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2017 2017
dbSNP: rs6059988
rs6059988 		20 34690297 intron variant T/C snv 0.41
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2018 2018