ClinVar Miner

List of variants reported as likely benign for homocystinuria by Counsyl

Included ClinVar conditions (21):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000071.3(CBS):c.1316G>A (p.Arg439Gln)	rs756467921	0.00003
NM_015506.3(MMACHC):c.603T>C (p.Arg201=)	rs398124294

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