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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130009662, TNFSF11
(E27G)
Single nucleotide variant
(missense variant +1 more)
not specified
+3 more
GBenign
LOC130009662, TNFSF11
(G28D)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
LOC130009662, TNFSF11
Single nucleotide variant
(synonymous variant +1 more)
not specified
+2 more
GBenign
LOC130009662, TNFSF11
Single nucleotide variant
(synonymous variant +1 more)
not specified
+2 more
GBenign
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