ClinVar Miner

List of variants in gene SAMHD1 reported as benign for Moyamoya syndrome

Included ClinVar conditions (54):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 1
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HGVS dbSNP
NM_015474.3(SAMHD1):c.1692C>T (p.Ala564=) rs200856791

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