List of variants in gene PROP1 reported as uncertain significance by Natera, Inc.

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_006261.5(PROP1):c.534G>A (p.Gln178=)	rs73807328	0.00184
NM_006261.5(PROP1):c.110-8G>A	rs377698903	0.00024
NM_006261.5(PROP1):c.234A>G (p.Pro78=)	rs533923552	0.00013
NM_006261.5(PROP1):c.303T>C (p.Ser101=)	rs114584451	0.00013
NM_006261.5(PROP1):c.624C>T (p.Cys208=)	rs761651134	0.00005
NM_006261.5(PROP1):c.249G>A (p.Gln83=)	rs373160119	0.00001
NM_006261.5(PROP1):c.131G>A (p.Arg44Lys)	rs1755702883
NM_006261.5(PROP1):c.152G>T (p.Gly51Val)	rs2233783
NM_006261.5(PROP1):c.51C>G (p.Val17=)	rs760446926

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