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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CYP7B1, LOC130000507
(R11L)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CYP7B1, LOC130000507
(A7P)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CYP7B1, LOC130000507
(S6C)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
CYP7B1, LOC130000507
(G3E)
Single nucleotide variant
(missense variant)
Spastic paraplegia
+1 more
GUncertain significance
CYP7B1, LOC130000507
Single nucleotide variant
(5 prime UTR variant)
not provided
+1 more
GUncertain significance
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