List of variants in gene PROP1 reported as uncertain significance by Eurofins NTD LLC (GA)

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_006261.5(PROP1):c.471C>T (p.Tyr157=)	rs145883811	0.00124
NM_006261.5(PROP1):c.96G>A (p.Pro32=)	rs144314831	0.00019
NM_006261.5(PROP1):c.423C>T (p.Ala141=)	rs200977367	0.00008
NM_006261.5(PROP1):c.193C>T (p.Arg65Cys)	rs767901591	0.00003
NM_006261.5(PROP1):c.550G>C (p.Ala184Pro)	rs746409513	0.00003
NM_006261.5(PROP1):c.52G>A (p.Gly18Ser)	rs775353413	0.00002
NM_006261.5(PROP1):c.456T>C (p.Ala152=)	rs758911793	0.00001
NM_006261.5(PROP1):c.339C>G (p.Ile113Met)	rs1562024419
NM_006261.5(PROP1):c.592T>C (p.Leu198=)	rs780774091
NM_006261.5(PROP1):c.636T>C (p.Pro212=)	rs759632048

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