ClinVar Miner

List of variants in gene combination GCH1, LOC130055692 reported as benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000161.3(GCH1):c.-40C>T	rs28458175	0.05363
NM_000161.3(GCH1):c.69C>T (p.Pro23=)	rs767294964	0.00023

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