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Items: 7

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NWD1
(Q183L +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GBenign
NWD1
(A77T +2 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
NWD1
(T205I +2 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
NWD1
(V588F +2 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
NWD1
Single nucleotide variant
(synonymous variant)
not provided
GBenign
NWD1
(G974S +2 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
ADGRE2, AKAP8
+57 more
Deletion
not provided
GUncertain significance
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