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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GYPB
(T58S)
Variation
(missense variant +1 more)
not provided
GBenign
GYPB
(C43W +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GYPB
(P32R +1 more)
Single nucleotide variant
(missense variant)
BLOOD GROUP, Ss
Gassociation
GYPB
(H28Y +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GYPB
(A26T)
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
GUncertain significance
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