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Links from MedGen

Items: 11

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ABCB6
(W64C)
Single nucleotide variant
(missense variant)
Dyschromatosis universalis hereditaria 3
GUncertain significance
ABCB6
Single nucleotide variant
(splice donor variant)
Dyschromatosis universalis hereditaria 3
GLikely pathogenic
ABCB6
(N631Y +1 more)
Single nucleotide variant
(missense variant)
Dyschromatosis universalis hereditaria 3
GUncertain significance
ABCB6
(V458A +1 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
ABCB6
Single nucleotide variant
(intron variant)
not provided
+4 more
GBenign/Likely benign
ABCB6
(V408A +1 more)
Single nucleotide variant
(missense variant)
Microphthalmia, isolated, with coloboma 7
+4 more
GConflicting classifications of pathogenicity
ABCB6
(R375W +1 more)
Single nucleotide variant
(missense variant)
Langereis blood group
+3 more
GLikely pathogenic
ABCB6
(Q555K +1 more)
Single nucleotide variant
(missense variant)
Dyschromatosis universalis hereditaria 3
GPathogenic
ABCB6
(G579E +1 more)
Single nucleotide variant
(missense variant)
Dyschromatosis universalis hereditaria 3
GPathogenic
ABCB6
(S170G)
Single nucleotide variant
(missense variant)
Dyschromatosis universalis hereditaria 3
GPathogenic
ABCB6
(L356P +1 more)
Single nucleotide variant
(missense variant)
Dyschromatosis universalis hereditaria 3
GPathogenic
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