List of variants in gene PRICKLE1 reported as benign for not provided

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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.1639+168G>C	rs2600924	0.97057
NM_153026.3(PRICKLE1):c.385-119A>C	rs2708062	0.96174
NM_153026.3(PRICKLE1):c.588+123C>G	rs2708061	0.96170
NM_153026.3(PRICKLE1):c.*91T>C	rs1043652	0.66849
NM_153026.3(PRICKLE1):c.247-248_247-247insG	rs3217624	0.60988
NM_153026.3(PRICKLE1):c.1902T>C (p.Ser634=)	rs3747562	0.45408
NM_153026.3(PRICKLE1):c.132+313G>A	rs1551210	0.33587
NM_153026.3(PRICKLE1):c.775+35T>C	rs12230583	0.33216
NM_153026.3(PRICKLE1):c.246+247C>T	rs3213989	0.32981
NM_153026.3(PRICKLE1):c.-49+129G>C	rs2141929	0.32281
NM_153026.3(PRICKLE1):c.1899T>C (p.Phe633=)	rs3747563	0.32044
NM_153026.3(PRICKLE1):c.*261T>C	rs1043656	0.29697
NM_153026.3(PRICKLE1):c.132+122T>C	rs2305422	0.14561
NM_153026.3(PRICKLE1):c.384+81G>C	rs67217830	0.12223
NM_153026.3(PRICKLE1):c.247-127C>T	rs67128387	0.08485
NM_153026.3(PRICKLE1):c.-48-343C>T	rs1037401	0.06692
NM_153026.3(PRICKLE1):c.-181G>A	rs117521428	0.05613
NM_153026.3(PRICKLE1):c.-48-293C>T	rs117438114	0.05309
NM_153026.3(PRICKLE1):c.1639+60A>C	rs58707767	0.04485
NM_153026.3(PRICKLE1):c.133-289del	rs139520280	0.03434
NM_153026.3(PRICKLE1):c.133-284G>A	rs113774118	0.02133
NM_153026.3(PRICKLE1):c.114G>A (p.Pro38=)	rs141743294	0.00302
NM_153026.3(PRICKLE1):c.177C>T (p.Tyr59=)	rs144843013	0.00149
GRCh37/hg19 12q12(chr12:42856396-42912131)x3
GRCh37/hg19 12q12(chr12:42865874-42899909)x3

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