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| Sick sinus syndrome v0.2 | GNB2 | Zornitza Stark Marked gene: GNB2 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sick sinus syndrome v0.2 | GNB2 | Zornitza Stark Gene: gnb2 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sick sinus syndrome v0.2 | GNB2 |
Zornitza Stark gene: GNB2 was added gene: GNB2 was added to Sick sinus syndrome. Sources: Expert list Mode of inheritance for gene: GNB2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: GNB2 were set to 28219978 Phenotypes for gene: GNB2 were set to Sick sinus syndrome 4, MIM# 619464 Review for gene: GNB2 was set to RED Added comment: Single large 3-generational family reported with a missense variant in this gene segregating with early and progressive sinus node and atrioventricular conduction dysfunction. Note recent reports of multiple individuals with syndromic ID and mono-allelic variants in this gene. Sources: Expert list |
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