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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129391057, MUC16
(T2506A +2 more)
Single nucleotide variant
(missense variant)
MUC16-related disorder
GBenign
LOC129391057, MUC16
Single nucleotide variant
(synonymous variant)
MUC16-related disorder
GLikely benign
LOC129391057, MUC16
(V2472I +2 more)
Single nucleotide variant
(missense variant)
MUC16-related disorder
+1 more
GBenign/Likely benign
LOC129391057, MUC16
(S2463L +2 more)
Single nucleotide variant
(missense variant)
MUC16-related disorder
GBenign
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