U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Links from MedGen

Items: 7

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC114827827, NPPA
+1 more
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 6
+2 more
GLikely benign
LOC114827827, NPPA
+1 more
(R107*)
Single nucleotide variant
(nonsense)
Atrial fibrillation, familial, 6
+1 more
GUncertain significance
LOC114827827, NPPA
(V9M)
Single nucleotide variant
(missense variant)
not specified
+2 more
GConflicting classifications of pathogenicity
LOC114827827, NPPA
+1 more
(P66L)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 6
+2 more
GUncertain significance
LOC114827827, NPPA
+1 more
(G85R)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 6
+1 more
GUncertain significance
LOC114827827, NPPA
+1 more
(S64R)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 6
+3 more
GBenign/Likely benign
LOC114827827, NPPA
+1 more
(R150Q)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 6
+1 more
GConflicting classifications of pathogenicity
Format
Items per page
Sort by
Choose Destination