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Items: 8

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FANCB
(T553M)
Single nucleotide variant
(missense variant)
FANCB-related condition
+3 more
GConflicting classifications of pathogenicity
FANCB
Single nucleotide variant
(synonymous variant)
not provided
+3 more
GConflicting classifications of pathogenicity
FANCB
Deletion
(intron variant)
Inborn genetic diseases
+5 more
GBenign
FANCB
Single nucleotide variant
(intron variant)
not specified
+4 more
GBenign
FANCB
(F380L)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+5 more
GConflicting classifications of pathogenicity
FANCB
Microsatellite
(intron variant)
Inborn genetic diseases
+2 more
GBenign/Likely benign
FANCB
Microsatellite
(intron variant)
FANCB-related condition
+5 more
GBenign/Likely benign
FANCB
(I330T)
Single nucleotide variant
(missense variant)
FANCB-related condition
+3 more
GConflicting classifications of pathogenicity
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