ClinVar Miner

List of variants reported as uncertain significance for Seckel syndrome 8 by Baylor Genetics

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 2
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HGVS dbSNP gnomAD frequency
NM_001080449.3(DNA2):c.2156G>T (p.Arg719Ile) rs2051805505
NM_001080449.3(DNA2):c.707T>C (p.Met236Thr) rs759464271

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