List of variants in gene PRICKLE2 reported as likely 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)
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_198859.4(PRICKLE2):c.-370G>A	rs139238137	0.00356
NM_198859.4(PRICKLE2):c.1527G>A (p.Glu509=)	rs144455095	0.00228
NM_198859.4(PRICKLE2):c.438G>A (p.Ala146=)	rs149786687	0.00113
NM_198859.4(PRICKLE2):c.1314G>C (p.Gln438His)	rs202170644	0.00064
NM_198859.4(PRICKLE2):c.2103G>T (p.Leu701=)	rs200220646	0.00014
NM_198859.4(PRICKLE2):c.474G>A (p.Pro158=)	rs771310187	0.00003
NM_198859.4(PRICKLE2):c.462C>T (p.Cys154=)	rs752867961	0.00001
NM_198859.4(PRICKLE2):c.516G>A (p.Leu172=)	rs727504105	0.00001
NM_198859.4(PRICKLE2):c.1896C>T (p.Asp632=)	rs773059932
NM_198859.4(PRICKLE2):c.2511G>A (p.Lys837=)	rs1474159913
NM_198859.4(PRICKLE2):c.330C>G (p.Arg110=)	rs751122249

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