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Items: 9

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
INF2
Single nucleotide variant
(synonymous variant)
Charcot-Marie-Tooth disease dominant intermediate E
+2 more
GBenign
INF2
Single nucleotide variant
(intron variant)
not specified
+2 more
GBenign
INF2
(A400T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
INF2
Single nucleotide variant
(synonymous variant)
Focal segmental glomerulosclerosis 5
+2 more
GBenign
INF2
Microsatellite
(inframe_deletion)
not specified
+2 more
GConflicting classifications of pathogenicity
INF2
Microsatellite
(inframe_deletion)
Focal segmental glomerulosclerosis 5
+3 more
GBenign
INF2
Deletion
(inframe_deletion)
not provided
+4 more
GBenign/Likely benign
INF2
(P516L)
Single nucleotide variant
(missense variant)
Focal segmental glomerulosclerosis 5
+3 more
GBenign
INF2
(R622G)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
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