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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCN5A
(T1620M +5 more)
Single nucleotide variant
(missense variant)
not provided
+9 more
GPathogenic/Likely pathogenic
SCN5A
(R1232W +2 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
SCN5A
(T512I)
Single nucleotide variant
(missense variant)
SUDDEN INFANT DEATH SYNDROME
+8 more
GUncertain significance
SCN5A
(R282H)
Single nucleotide variant
(missense variant)
Cardiac arrhythmia
+2 more
GPathogenic/Likely pathogenic
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