ClinVar Miner

List of variants in gene FGFR1, LOC102723716 studied for Pfeiffer syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NM_023110.3(FGFR1):c.*2104del	rs201364530	0.00099

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