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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC9A1
(V286M)
Single nucleotide variant
(missense variant +1 more)
Lichtenstein-Knorr syndrome
+1 more
GUncertain significance
SLC9A1
(G215D)
Single nucleotide variant
(missense variant)
Lichtenstein-Knorr syndrome
GUncertain significance