ClinVar Miner

List of variants in gene NPTX1 reported as benign for not provided

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_002522.4(NPTX1):c.1041C>T (p.Ile347=)	rs34937624	0.03119
NM_002522.4(NPTX1):c.309G>A (p.Arg103=)	rs201541109	0.01585

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