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Items: 6

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
B4GALT1
Indel
(intron variant +1 more)
not provided
GUncertain significance
B4GALT1
Single nucleotide variant
(synonymous variant +1 more)
not provided
GUncertain significance
B4GALT1
Single nucleotide variant
(synonymous variant +1 more)
not provided
GUncertain significance
B4GALT1
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign
B4GALT1
(V173I +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
B4GALT1
Duplication
(intron variant)
not provided
GConflicting classifications of pathogenicity
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