List of variants in gene PRPH2 reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000322.5(PRPH2):c.708C>T (p.Tyr236=)	rs61755813	0.00062
NM_000322.5(PRPH2):c.249C>T (p.Tyr83=)	rs61755775	0.00053
NM_000322.5(PRPH2):c.300G>A (p.Pro100=)	rs150695654	0.00011
NM_000322.5(PRPH2):c.408C>T (p.Asn136=)	rs148513859	0.00004
NM_000322.5(PRPH2):c.801C>T (p.Val267=)	rs189358082	0.00002
NM_000322.5(PRPH2):c.435C>T (p.Asp145=)
NM_000322.5(PRPH2):c.864G>A (p.Thr288=)

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