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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129998833, SLC25A13
(M1K)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
LOC129998833, SLC25A13
(M1T)
Single nucleotide variant
(missense variant +2 more)
not provided
+6 more
GUncertain significance