NFS1, NFS1 cysteine desulfurase, 9054

N. diseases: 8; N. variants: 9
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: rs11907022
rs11907022 		20 35695704 intron variant A/G snv 0.10
CUI: C0919677
Disease: Protein C measurement
Protein C measurement 		0.700 1.000 1 2010 2010
dbSNP: rs11907022
rs11907022 		20 35695704 intron variant A/G snv 0.10
CUI: C1168438
Disease: Protein C antigen measurement
Protein C antigen measurement 		0.700 1.000 1 2010 2010
dbSNP: rs17336615
rs17336615 		20 35674089 non coding transcript exon variant A/C;G snv
CUI: C0919677
Disease: Protein C measurement
Protein C measurement 		0.700 1.000 1 2010 2010
dbSNP: rs17336615
rs17336615 		20 35674089 non coding transcript exon variant A/C;G snv
CUI: C1168438
Disease: Protein C antigen measurement
Protein C antigen measurement 		0.700 1.000 1 2010 2010
dbSNP: rs2180280
rs2180280 		20 35669429 3 prime UTR variant T/C snv 6.7E-02
CUI: C1168438
Disease: Protein C antigen measurement
Protein C antigen measurement 		0.700 1.000 1 2010 2010
dbSNP: rs2180280
rs2180280 		20 35669429 3 prime UTR variant T/C snv 6.7E-02
CUI: C0919677
Disease: Protein C measurement
Protein C measurement 		0.700 1.000 1 2010 2010
dbSNP: rs3088078
rs3088078 		20 35700932 3 prime UTR variant C/T snv 6.0E-02 3.7E-02
CUI: C0919677
Disease: Protein C measurement
Protein C measurement 		0.700 1.000 1 2010 2010
dbSNP: rs3088078
rs3088078 		20 35700932 3 prime UTR variant C/T snv 6.0E-02 3.7E-02
CUI: C1168438
Disease: Protein C antigen measurement
Protein C antigen measurement 		0.700 1.000 1 2010 2010
dbSNP: rs6060546
rs6060546 		20 35669741 intron variant A/C;G snv
CUI: C1168438
Disease: Protein C antigen measurement
Protein C antigen measurement 		0.700 1.000 1 2010 2010
dbSNP: rs6060546
rs6060546 		20 35669741 intron variant A/C;G snv
CUI: C0919677
Disease: Protein C measurement
Protein C measurement 		0.700 1.000 1 2010 2010
dbSNP: rs6060548
rs6060548 		20 35676643 intron variant T/A snv 6.7E-02
CUI: C0919677
Disease: Protein C measurement
Protein C measurement 		0.700 1.000 1 2010 2010
dbSNP: rs6060548
rs6060548 		20 35676643 intron variant T/A snv 6.7E-02
CUI: C1168438
Disease: Protein C antigen measurement
Protein C antigen measurement 		0.700 1.000 1 2010 2010
dbSNP: rs6121023
rs6121023 		20 35668718 3 prime UTR variant A/C snv 6.7E-02
CUI: C1168438
Disease: Protein C antigen measurement
Protein C antigen measurement 		0.700 1.000 1 2010 2010
dbSNP: rs6121023
rs6121023 		20 35668718 3 prime UTR variant A/C snv 6.7E-02
CUI: C0919677
Disease: Protein C measurement
Protein C measurement 		0.700 1.000 1 2010 2010
dbSNP: rs6121029
rs6121029 		20 35686515 intron variant T/C snv 0.10
CUI: C0919677
Disease: Protein C measurement
Protein C measurement 		0.700 1.000 1 2010 2010
dbSNP: rs6121029
rs6121029 		20 35686515 intron variant T/C snv 0.10
CUI: C1168438
Disease: Protein C antigen measurement
Protein C antigen measurement 		0.700 1.000 1 2010 2010
dbSNP: rs6060566
rs6060566 		0.925 0.160 20 35700304 intron variant T/C snv 0.19
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs6060566
rs6060566 		0.925 0.160 20 35700304 intron variant T/C snv 0.19
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy 		Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases 0.010 1.000 1 2015 2015