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Items: 12

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GP6
(F606L)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GBenign
GP6
(R573G)
Single nucleotide variant
(missense variant +1 more)
Platelet-type bleeding disorder 11
+2 more
GBenign
GP6
Single nucleotide variant
(synonymous variant +1 more)
not specified
+2 more
GBenign
GP6
(K323T +2 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign
GP6
(L299Q +1 more)
Single nucleotide variant
(synonymous variant +1 more)
Platelet-type bleeding disorder 11
+2 more
GBenign
GP6
(P314A)
Single nucleotide variant
(missense variant +1 more)
Platelet-type bleeding disorder 11
+1 more
GBenign
GP6
(A231T +1 more)
Single nucleotide variant
(missense variant)
Platelet-type bleeding disorder 11
+2 more
GBenign
GP6
(E219K +1 more)
Single nucleotide variant
(missense variant)
Platelet-type bleeding disorder 11
+2 more
GBenign
GP6
(P219S)
Single nucleotide variant
(missense variant +1 more)
not specified
+2 more
GBenign
GP6
Single nucleotide variant
(synonymous variant)
Platelet-type bleeding disorder 11
+2 more
GBenign
GP6
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign
GP6
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign
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