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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129993885, NDUFS4
Single nucleotide variant
(synonymous variant +1 more)
not provided
+2 more
GBenign
NDUFS4
Single nucleotide variant
(synonymous variant +1 more)
Leigh syndrome
+3 more
GBenign
NDUFS4
Single nucleotide variant
(synonymous variant +1 more)
Leigh syndrome
+2 more
GBenign
NDUFS4
Duplication
(intron variant)
Leigh syndrome
+4 more
GBenign/Likely benign
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