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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130056709, NIPA1
Microsatellite
(inframe_insertion +1 more)
not specified
+3 more
GBenign/Likely benign
LOC130056709, NIPA1
Microsatellite
(inframe_insertion +1 more)
Spastic paraplegia, autosomal dominant
+4 more
GConflicting classifications of pathogenicity
LOC130056709, NIPA1
Microsatellite
(inframe_deletion +1 more)
not specified
+2 more
GBenign/Likely benign
LOC130056709, NIPA1
(A16del)
Microsatellite
(inframe_deletion +1 more)
Spastic paraplegia, autosomal dominant
+3 more
GBenign/Likely benign
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