U.S. flag

An official website of the United States government

Search results

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GRN
(V77I)
Single nucleotide variant
(missense variant)
GRN-related frontotemporal lobar degeneration with Tdp43 inclusions
+3 more
GUncertain significance
GRN
(P127A)
Single nucleotide variant
(missense variant)
GRN-related frontotemporal lobar degeneration with Tdp43 inclusions
+2 more
GUncertain significance
GRN
(Q130fs)
Deletion
(frameshift variant)
GRN-related frontotemporal lobar degeneration with Tdp43 inclusions
+4 more
GPathogenic
GRN
(C158Y)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GRN
(M207T)
Single nucleotide variant
(missense variant)
GRN-related frontotemporal lobar degeneration with Tdp43 inclusions
+2 more
GUncertain significance
GRN, LOC125177489
(P233Q)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+3 more
GUncertain significance
GRN
Single nucleotide variant
(intron variant)
GRN-related frontotemporal lobar degeneration with Tdp43 inclusions
+2 more
GConflicting classifications of pathogenicity
GRN
(R579H)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+3 more
GUncertain significance
GRN
Deletion
not specified
GUncertain significance
External link. Please review our privacy policy.