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Items: 10

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ZFAND2A
(A113G +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ZFAND2A
(G120S)
Single nucleotide variant
(missense variant +2 more)
Inborn genetic diseases
GUncertain significance
ZFAND2A
(R99H)
Single nucleotide variant
(missense variant +2 more)
Inborn genetic diseases
GUncertain significance
ZFAND2A
(G89A)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ZFAND2A
(G77A)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ZFAND2A
(K50R)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ZFAND2A
(P45L)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ZFAND2A
(C33G)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ZFAND2A
(K29E)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ZFAND2A
(A27V)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
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