List of variants in gene PRICKLE1 reported as uncertain significance by GeneDx

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: 25

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HGVS	dbSNP	gnomAD frequency
NM_153026.3(PRICKLE1):c.2404C>T (p.Pro802Ser)	rs150545495	0.00160
NM_153026.3(PRICKLE1):c.2216C>T (p.Ser739Phe)	rs138452760	0.00062
NM_153026.3(PRICKLE1):c.2269G>A (p.Glu757Lys)	rs145860632	0.00037
NM_153026.3(PRICKLE1):c.1547G>C (p.Trp516Ser)	rs139901494	0.00014
NM_153026.3(PRICKLE1):c.25A>G (p.Met9Val)	rs566073131	0.00012
NM_153026.3(PRICKLE1):c.391T>G (p.Leu131Val)	rs35731866	0.00011
NM_153026.3(PRICKLE1):c.113C>T (p.Pro38Leu)	rs145493619	0.00010
NM_153026.3(PRICKLE1):c.132G>A (p.Gln44=)	rs377668062	0.00005
NM_153026.3(PRICKLE1):c.2105G>A (p.Arg702Gln)	rs369790443	0.00005
NM_153026.3(PRICKLE1):c.431G>A (p.Arg144His)	rs281865563	0.00004
NM_153026.3(PRICKLE1):c.1676C>T (p.Ser559Leu)	rs771584708	0.00003
NM_153026.3(PRICKLE1):c.2224G>A (p.Gly742Ser)	rs370967125	0.00003
NM_153026.3(PRICKLE1):c.1360G>A (p.Glu454Lys)	rs748454609	0.00002
NM_153026.3(PRICKLE1):c.100G>A (p.Ala34Thr)	rs781255236	0.00001
NM_153026.3(PRICKLE1):c.1444G>A (p.Asp482Asn)	rs1555229983	0.00001
NM_153026.3(PRICKLE1):c.1516G>A (p.Ala506Thr)	rs796052932	0.00001
NM_153026.3(PRICKLE1):c.1888C>G (p.Gln630Glu)	rs200171609	0.00001
NM_153026.3(PRICKLE1):c.2045G>A (p.Arg682His)	rs189093086	0.00001
NM_153026.3(PRICKLE1):c.2330A>G (p.Tyr777Cys)	rs768039518	0.00001
NM_153026.3(PRICKLE1):c.101C>T (p.Ala34Val)	rs139176541
NM_153026.3(PRICKLE1):c.1960G>A (p.Glu654Lys)	rs1555229356
NM_153026.3(PRICKLE1):c.2167G>A (p.Ala723Thr)	rs796052933
NM_153026.3(PRICKLE1):c.425C>T (p.Ala142Val)	rs796052928
NM_153026.3(PRICKLE1):c.713T>C (p.Phe238Ser)	rs796052930
NM_153026.3(PRICKLE1):c.8del (p.Leu3fs)	rs754532709

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