ClinVar Miner

Submissions for variant NM_030777.4(SLC2A10):c.1334G>A (p.Gly445Glu)

gnomAD frequency: 0.00001 dbSNP: rs753723351

Minimum review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total submissions: 1

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
GeneReviews	RCV000202473	SCV000195656	not provided	Arterial tortuosity syndrome		no assertion provided	literature only

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