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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC1A3
(R23H)
Single nucleotide variant
(missense variant)
Episodic ataxia type 6
+1 more
GBenign/Likely benign
SLC1A3
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GBenign/Likely benign
SLC1A3
(F170L +1 more)
Single nucleotide variant
(missense variant)
Episodic ataxia type 6
+1 more
GUncertain significance
SLC1A3
Single nucleotide variant
(intron variant)
not specified
+2 more
GBenign/Likely benign
SLC1A3
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GBenign/Likely benign
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