SLC10A1, solute carrier family 10 member 1, 6554

N. diseases: 54; N. variants: 7
Disease: Indirect Hyperbilirubinemia, Neonatal ×
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: rs148467625
rs148467625 		1.000 0.080 14 69796893 missense variant A/G snv 1.4E-03 7.3E-04
CUI: C1565886
Disease: Indirect Hyperbilirubinemia, Neonatal
Indirect Hyperbilirubinemia, Neonatal 		Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities 0.010 1.000 1 2017 2017