U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Search results

Items: 25

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCNV2
(W16C)
Single nucleotide variant
(missense variant)
Cone dystrophy with supernormal rod response
+2 more
GUncertain significance
KCNV2
(E20K)
Single nucleotide variant
(missense variant)
KCNV2-related condition
+2 more
GBenign/Likely benign
KCNV2
(R27H)
Single nucleotide variant
(missense variant)
KCNV2-related condition
+3 more
GConflicting classifications of pathogenicity
KCNV2
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GBenign
KCNV2
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
KCNV2
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign
KCNV2
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
KCNV2
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign/Likely benign
KCNV2
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
KCNV2
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GBenign
KCNV2
(D147E)
Single nucleotide variant
(missense variant)
not provided
GConflicting classifications of pathogenicity
KCNV2
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GBenign/Likely benign
KCNV2
(K215N)
Single nucleotide variant
(missense variant)
KCNV2-related condition
+3 more
GBenign/Likely benign
KCNV2
(V226I)
Single nucleotide variant
(missense variant)
not provided
+2 more
GBenign
KCNV2
(M236V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KCNV2
(P241S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KCNV2
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
KCNV2
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign
KCNV2
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign
KCNV2
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign
KCNV2
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
KCNV2
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign/Likely benign
KCNV2
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign/Likely benign
KCNV2
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
KCNV2
(G421D)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
Format
Items per page
Sort by
Choose Destination