RS370933531 RIPPLY2

Health Risk Chr 6:83857238
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What This Variant Does
"CLNSIG=5
Associated Conditions
Spondylocostal dysostosis 6
autosomal recessive
Spondylocostal dysostosis 2
RIPPLY2-related disorder
Spondylocostal dysostosis 6
autosomal recessive
Spondylocostal dysostosis 2
RIPPLY2-related disorder
Other Variants in RIPPLY2
rs864309489 rs201419367
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