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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLCO1B3, SLCO1B3-SLCO1B7
(I168T +1 more)
Single nucleotide variant
(missense variant)
Rotor syndrome
GUncertain significance
SLCO1B3, SLCO1B3-SLCO1B7
(I215M +1 more)
Single nucleotide variant
(missense variant)
Rotor syndrome
GUncertain significance
SLCO1B3, SLCO1B3-SLCO1B7
(G409S +1 more)
Single nucleotide variant
(missense variant)
Rotor syndrome
GUncertain significance
SLCO1B3, SLCO1B3-SLCO1B7
Single nucleotide variant
(splice donor variant)
Rotor syndrome
GPathogenic
SLCO1B1
(T531R)
Single nucleotide variant
(missense variant)
Rotor syndrome
GUncertain significance
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