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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MRE11
Single nucleotide variant
(intron variant)
not specified
+4 more
GBenign
MRE11
(R502C)
Single nucleotide variant
(missense variant)
Ataxia-telangiectasia-like disorder
+5 more
GConflicting classifications of pathogenicity
MRE11
Single nucleotide variant
(synonymous variant)
MRE11-related condition
+6 more
GBenign
MRE11
Deletion
(intron variant)
Ataxia-telangiectasia-like disorder
+3 more
GBenign/Likely benign
MRE11
Single nucleotide variant
(synonymous variant)
Ataxia-telangiectasia-like disorder
+4 more
GConflicting classifications of pathogenicity
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