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Items: 9

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ADAM9, LOC130000261
Single nucleotide variant
(synonymous variant +1 more)
not provided
+2 more
GBenign
ADAM9
(E76K)
Single nucleotide variant
(missense variant +1 more)
not specified
+2 more
GBenign/Likely benign
ADAM9
(V94I)
Single nucleotide variant
(missense variant +1 more)
not provided
+3 more
GConflicting classifications of pathogenicity
ADAM9
(E100V)
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
GUncertain significance
ADAM9
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
GConflicting classifications of pathogenicity
ADAM9
Single nucleotide variant
(synonymous variant +1 more)
not provided
GConflicting classifications of pathogenicity
ADAM9
Duplication
(intron variant)
not specified
+1 more
GBenign/Likely benign
ADAM9
(N631K)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ADAM9
Single nucleotide variant
(synonymous variant +1 more)
not provided
GConflicting classifications of pathogenicity
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