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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130008356, POC1B
+1 more
Single nucleotide variant
(intron variant)
not provided
GLikely benign
LOC130008357, POC1B
+2 more
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
GBenign
LOC130008357, POC1B
+2 more
Duplication
(intron variant)
not provided
GLikely benign
POC1B-GALNT4, LOC130008357
+2 more
Deletion
(intron variant)
not provided
GBenign
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