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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCN11A
Single nucleotide variant
(synonymous variant)
not provided
+3 more
GBenign/Likely benign
SCN11A
Single nucleotide variant
(synonymous variant)
not provided
+3 more
GBenign/Likely benign
SCN11A
Single nucleotide variant
(synonymous variant)
Familial episodic pain syndrome with predominantly lower limb involvement
+2 more
GConflicting classifications of pathogenicity
SCN11A
(G168fs)
Duplication
(frameshift variant)
not provided
+3 more
GConflicting classifications of pathogenicity
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