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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RANGRF, SLC25A35
+1 more
(V42L)
Single nucleotide variant
(missense variant +3 more)
RANGRF-related condition
+1 more
GLikely benign
RANGRF, SLC25A35
(E61*)
Single nucleotide variant
(nonsense +3 more)
Cardiac arrhythmia
+3 more
GBenign/Likely benign
RANGRF, SLC25A35
(V269M)
Single nucleotide variant
(3 prime UTR variant +3 more)
Cardiac arrhythmia
+1 more
GLikely benign
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