List of variants in gene combination CCNH, RASA1 reported as uncertain significance for Parkes Weber syndrome

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)
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_002890.3(RASA1):c.*298T>C	rs886060846	0.00006
NM_002890.3(RASA1):c.*16T>C	rs770822619	0.00004
NM_002890.3(RASA1):c.2608T>C (p.Leu870=)	rs372498033	0.00004
NM_002890.3(RASA1):c.*448T>G	rs886060847	0.00001
NM_002890.3(RASA1):c.*9G>A	rs886060845	0.00001
NM_002890.3(RASA1):c.1305T>C (p.Tyr435=)	rs778801311	0.00001
NM_002890.3(RASA1):c.2926-14C>T	rs886060843	0.00001
NM_002890.3(RASA1):c.3029G>A (p.Arg1010Gln)	rs886060844	0.00001
NM_002890.3(RASA1):c.*1000GTTAA[1]	rs886060850
NM_002890.3(RASA1):c.*424G>A	rs191725379
NM_002890.3(RASA1):c.*572C>A	rs886060848
NM_002890.3(RASA1):c.*840ATT[1]	rs201705926
NM_002890.3(RASA1):c.2011+4A>C	rs886060840
NM_002890.3(RASA1):c.2049G>C (p.Gly683=)	rs886060841
NM_002890.3(RASA1):c.2487+11A>C	rs886060842
NM_002890.3(RASA1):c.899+8A>G	rs781285667

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