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Items: 10

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WDPCP
Single nucleotide variant
(intron variant)
Bardet-Biedl syndrome 15
+5 more
GBenign
WDPCP
Single nucleotide variant
(synonymous variant +1 more)
not specified
+3 more
GConflicting classifications of pathogenicity
WDPCP
(L532del +2 more)
Microsatellite
(inframe_deletion +1 more)
Bardet-Biedl syndrome 15
+3 more
GUncertain significance
WDPCP
(A445P +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+3 more
GBenign/Likely benign
WDPCP
(S330L +2 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
WDPCP
Single nucleotide variant
(synonymous variant +1 more)
not provided
GUncertain significance
WDPCP
(L129V +1 more)
Single nucleotide variant
(missense variant +1 more)
Bardet-Biedl syndrome
+1 more
GLikely benign
WDPCP
Deletion
(intron variant)
Bardet-Biedl syndrome
+1 more
GBenign/Likely benign
WDPCP
(P23Q)
Single nucleotide variant
(5 prime UTR variant +2 more)
not provided
+3 more
GBenign/Likely benign
WDPCP
(F5L)
Single nucleotide variant
(5 prime UTR variant +2 more)
WDPCP-related condition
+3 more
GConflicting classifications of pathogenicity
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