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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130009662, TNFSF11
(E27G)
Single nucleotide variant
(missense variant +1 more)
Increased bone mineral density
+3 more
GBenign
LOC130009662, TNFSF11
(P36R)
Single nucleotide variant
(missense variant +1 more)
not provided
+3 more
GBenign/Likely benign