ClinVar Miner

List of variants reported as pathogenic for Acroosteolysis dominant type by OMIM

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 7
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HGVS dbSNP gnomAD frequency
NM_024408.4(NOTCH2):c.6272del (p.Phe2091fs) rs1557802353
NM_024408.4(NOTCH2):c.6622C>T (p.Gln2208Ter) rs387906746
NM_024408.4(NOTCH2):c.6895G>T (p.Glu2299Ter) rs387906748
NM_024408.4(NOTCH2):c.6949C>T (p.Gln2317Ter) rs387906747
NM_024408.4(NOTCH2):c.7119T>G (p.Tyr2373Ter) rs1557801639
NM_024408.4(NOTCH2):c.7165C>T (p.Gln2389Ter) rs387906749
NOTCH2, 1-BP DEL, 6460T

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