Variants in gene PCCA with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 9

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HGVS	dbSNP	gnomAD frequency
NM_000282.4(PCCA):c.1651G>T (p.Val551Phe)	rs61749895	0.00606
NM_000282.4(PCCA):c.231+15C>T	rs202049874	0.00291
NM_000282.4(PCCA):c.1236A>G (p.Pro412=)	rs41281120	0.00219
NM_000282.4(PCCA):c.828T>C (p.Gly276=)	rs143838146	0.00143
NM_000282.4(PCCA):c.1676G>T (p.Trp559Leu)	rs118169528	0.00088
NM_000282.4(PCCA):c.1850T>C (p.Leu617Pro)	rs563417983	0.00028
NM_000282.4(PCCA):c.36C>T (p.Val12=)	rs375516917	0.00009
NM_000282.4(PCCA):c.2017G>C (p.Val673Leu)	rs142646074
NM_000282.4(PCCA):c.929C>G (p.Ala310Gly)	rs146927771

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