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Items: 15

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RIMS1
(P10S)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
RIMS1
(V57L)
Single nucleotide variant
(missense variant +1 more)
Cone-rod dystrophy 7
+2 more
GConflicting classifications of pathogenicity
RIMS1
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign
RIMS1
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GBenign
RIMS1
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GLikely benign
RIMS1
Single nucleotide variant
(synonymous variant)
RIMS1-related condition
+1 more
GConflicting classifications of pathogenicity
RIMS1
Single nucleotide variant
(synonymous variant +1 more)
not provided
GConflicting classifications of pathogenicity
RIMS1
(S703T +4 more)
Single nucleotide variant
(missense variant)
not provided
GConflicting classifications of pathogenicity
RIMS1
Single nucleotide variant
(intron variant)
not provided
+1 more
GConflicting classifications of pathogenicity
RIMS1
(P965L +8 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
RIMS1
Single nucleotide variant
(intron variant)
not provided
+1 more
GConflicting classifications of pathogenicity
RIMS1
(S1262L +39 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
RIMS1
Single nucleotide variant
(intron variant)
RIMS1-related condition
+1 more
GConflicting classifications of pathogenicity
RIMS1
(T1536A +62 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
RIMS1
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GBenign
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