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Items: 6

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCN10A
(A1886V +2 more)
Single nucleotide variant
(missense variant)
SCN10A-related condition
+4 more
GBenign/Likely benign
SCN10A
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+3 more
GBenign
SCN10A
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign
SCN10A
(V1287I +2 more)
Single nucleotide variant
(missense variant)
SCN10A-related condition
+4 more
GConflicting classifications of pathogenicity
LOC110121288, SCN10A
(I962V +1 more)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+3 more
GBenign/Likely benign
SCN10A
(R485C)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+3 more
GBenign/Likely benign
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