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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
B9D1, LOC130060455
Single nucleotide variant
(synonymous variant +1 more)
Meckel syndrome, type 9
+2 more
GConflicting classifications of pathogenicity
B9D1, LOC130060455
Single nucleotide variant
(5 prime UTR variant +1 more)
Meckel syndrome, type 9
GUncertain significance
B9D1, LOC130060455
Single nucleotide variant
(5 prime UTR variant +1 more)
Meckel syndrome, type 9
GUncertain significance
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