ClinVar Miner

List of variants reported as pathogenic for non-syndromic synpolydactyly by Fulgent Genetics, Fulgent Genetics

Included ClinVar conditions (8):

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000523.4(HOXD13):c.820C>T (p.Arg274Ter)	rs200750564	0.00001
NM_000168.6(GLI3):c.1880_1881del (p.His627fs)	rs2128710014
NM_000523.4(HOXD13):c.183_206dup (p.Ala64_Ala71dup)	rs756844068

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