ClinVar Miner

List of variants in gene DLL3 reported as benign for autosomal recessive spondylocostal dysostosis

Included ClinVar conditions (5):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
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HGVS dbSNP gnomAD frequency
NM_203486.3(DLL3):c.653T>C (p.Leu218Pro) rs1110627 0.59676
NM_203486.3(DLL3):c.352-18C>G rs2304223 0.29309
NM_203486.3(DLL3):c.1029C>T (p.Pro343=) rs2304214 0.27957
NM_203486.3(DLL3):c.1152G>A (p.Ala384=) rs115456333 0.01391
NM_203486.3(DLL3):c.1674-10C>T rs116099821 0.00950
NM_203486.3(DLL3):c.674G>A (p.Ser225Asn) rs35380611 0.00724
NM_203486.3(DLL3):c.1143C>T (p.Ala381=) rs367573123 0.00458
NM_203486.3(DLL3):c.160C>A (p.Leu54Ile) rs200673897 0.00285
NM_203486.3(DLL3):c.390G>A (p.Glu130=) rs113780398 0.00200

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