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Items: 6

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
VPS37A
Single nucleotide variant
(5 prime UTR variant)
not specified
GBenign/Likely benign
VPS37A
(G21S)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
VPS37A
Single nucleotide variant
(synonymous variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
VPS37A
Single nucleotide variant
(synonymous variant +1 more)
not specified
+1 more
GBenign
VPS37A
(P138S +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
VPS37A
(I213V +2 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign/Likely benign
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