ClinVar Miner

List of variants studied for 22q11.2 deletion syndrome by Fulgent Genetics,Fulgent Genetics

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 1
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HGVS dbSNP
NM_080647.1(TBX1):c.1049G>A (p.Gly350Asp) rs781731042

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