SLC10A1, solute carrier family 10 member 1, 6554

N. diseases: 54; N. variants: 7
Disease: Hepatitis B ×
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: rs2296651
rs2296651 		0.732 0.240 14 69778476 missense variant G/A snv 6.3E-03 2.5E-03
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.100 0.938 16 2014 2019
dbSNP: rs201339654
rs201339654 		0.925 0.080 14 69786192 missense variant C/G;T snv 8.0E-06; 2.0E-05
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.010 1.000 1 2018 2018
dbSNP: rs4646285
rs4646285 		1.000 0.080 14 69796931 synonymous variant C/T snv 9.7E-02 7.2E-02
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.010 1.000 1 2018 2018
dbSNP: rs4646287
rs4646287 		0.925 0.120 14 69796098 intron variant C/T snv 3.3E-03
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.010 1.000 1 2016 2016
dbSNP: rs7154439
rs7154439 		0.925 0.120 14 69799111 upstream gene variant G/A snv 0.36
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.010 1.000 1 2014 2014
dbSNP: rs943277
rs943277 		1.000 0.080 14 69794608 intron variant G/A snv 0.13
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.010 1.000 1 2017 2017