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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
APBA1, BANCR
+40 more
Copy number loss
See cases
GPathogenic
LOC130001862, FXN
(L4fs)
Microsatellite
(frameshift variant)
not provided
+2 more
GPathogenic/Likely pathogenic
LOC130001862, FXN
Single nucleotide variant
(synonymous variant)
not provided
+3 more
GBenign
FXN, LOC130001862
(G38S)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
LOC130001862, FXN
(R40C)
Single nucleotide variant
(missense variant)
not specified
+3 more
GUncertain significance
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