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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130002133, PTCH1
Microsatellite
(5 prime UTR variant +2 more)
Hereditary cancer-predisposing syndrome
+3 more
GBenign/Likely benign
LOC130002133, PTCH1
Microsatellite
(5 prime UTR variant +2 more)
PTCH1-related condition
+4 more
GBenign
LOC130002133, PTCH1
Microsatellite
(5 prime UTR variant +2 more)
Hereditary cancer-predisposing syndrome
+2 more
GBenign/Likely benign
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