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Items: 62

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ABHD8, ACP5
+2135 more
Copy number gain
See cases
GPathogenic
LOC129391074, LOC130063625
+351 more
Copy number gain
See cases
GPathogenic
ADGRE2, ADGRE3
+318 more
Copy number loss
See cases
GPathogenic
ADGRE2, ADGRE3
+180 more
Copy number loss
See cases
GPathogenic
ABHD8, ADGRE2
+695 more
Copy number gain
See cases
GPathogenic
ADGRE2, ADGRE3
+237 more
Copy number loss
See cases
GPathogenic
LOC130063788, LOC130063789
+77 more
Copy number loss
See cases
GUncertain significance
ADGRE2, ADGRE3
+41 more
Copy number gain
See cases
GUncertain significance
ADGRE3, CLEC17A
(R279W)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADGRE3, CLEC17A
(R318G)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
ADGRE3, CLEC17A
(A319T)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
ADGRE3, CLEC17A
(T368M)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
ADGRE3
(K505M +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADGRE3
(W612C +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADGRE3
(K611E +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADGRE3
(Q603H +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADGRE3
(G465A +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADGRE3
(S462R +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADGRE3
(G442D +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADGRE3
(M423V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADGRE3
(E414K +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADGRE3
(I389T +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADGRE3
(H436Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADGRE3
(W360C +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADGRE3
(T383S +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADGRE3
(P289H +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADGRE3
(E288G +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADGRE3
(C272R +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADGRE3
(S344L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADGRE3
(L254P +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADGRE3
(V314I +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADGRE3
(D227Y +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADGRE3
(E300D +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADGRE3
(M345L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADGRE3
(Y254S +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADGRE3
(V167M +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADGRE3
(T161M +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADGRE3
(S155Y +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADGRE3
(S229C +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADGRE3
(G149A +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADGRE3
(V263M +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADGRE3
(M131T +2 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ADGRE3
(I111T +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADGRE3
(G229R +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADGRE3
(S172N +2 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ADGRE3
(N159S +2 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ADGRE3
(C203R +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADGRE3
(A198V +2 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ADGRE3
(K86R +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADGRE3
(K134N +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADGRE3
(N87K)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADGRE3
(N69K)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADGRE3
(F60L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADGRE3
(K56E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADGRE3
(C37W)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CYP4F8, DCAF15
+109 more
Copy number gain
not specified
GUncertain significance
ADGRE2, ADGRE3
+55 more
Copy number loss
not specified
GPathogenic
BST2, NWD1
+158 more
Copy number gain
not provided
GPathogenic
ADGRE2, ADGRE3
+30 more
Copy number loss
not provided
GPathogenic
PGLYRP1, PGLYRP2
+1364 more
Copy number gain
See cases
GPathogenic
TMC4, TMED1
+1364 more
Copy number gain
See cases
GPathogenic
ADGRL1, ANGPTL6
+153 more
Copy number gain
See cases
GPathogenic
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