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Items: 6

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MAPT
(G213R +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GBenign/Likely benign
MAPT
(Q230R +1 more)
Single nucleotide variant
(missense variant +1 more)
Frontotemporal dementia
+6 more
GBenign/Likely benign
MAPT
(Y441H +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+2 more
GBenign
MAPT
Single nucleotide variant
(synonymous variant +1 more)
not specified
+2 more
GBenign
MAPT
Single nucleotide variant
(synonymous variant +1 more)
not provided
+3 more
GBenign
MAPT
Single nucleotide variant
(intron variant)
Inborn genetic diseases
+3 more
GBenign/Likely benign
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