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Links from MedGen

Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HSPA9
Single nucleotide variant
(synonymous variant)
Autosomal dominant sideroblastic anemia
+2 more
GBenign/Likely benign
HSPA9
Deletion
(inframe_deletion)
Autosomal dominant sideroblastic anemia
GPathogenic
HSPA9
Deletion
(nonsense)
Autosomal dominant sideroblastic anemia
GPathogenic
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