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Items: 11

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ABCA2, LINC02908
(M1V)
Single nucleotide variant
(missense variant +1 more)
not provided
GBenign
FUT7, LINC02908
(Y324H)
Single nucleotide variant
(missense variant)
not provided
GBenign
FUT7, LINC02908
(G249S)
Single nucleotide variant
(missense variant)
not provided
GBenign
HMCN2, IER5L
+147 more
Duplication
not provided
GUncertain significance
STKLD1, STPG3
+110 more
Duplication
Kleefstra syndrome 1
GUncertain significance
ABCA2, AGPAT2
+85 more
Deletion
Developmental and epileptic encephalopathy, 14
+3 more
GConflicting classifications of pathogenicity
ABCA2, ABL1
+187 more
Duplication
Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome
GUncertain significance
ABCA2, AGPAT2
+73 more
Deletion
Rafiq syndrome
GPathogenic
ABCA2, ABO
+100 more
Duplication
Developmental and epileptic encephalopathy, 14
+4 more
GUncertain significance
ABCA2, AGPAT2
+49 more
Duplication
Developmental and epileptic encephalopathy, 14
+2 more
GUncertain significance
LCN12, LCN15
+77 more
Deletion
Kleefstra syndrome 1
+2 more
GConflicting classifications of pathogenicity
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