List of variants in gene PPP1R12A reported as likely pathogenic for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_002480.3(PPP1R12A):c.1823+2T>C	rs61756421	0.00013
GRCh37/hg19 12q21.2(chr12:80187643-80222244)x1
NM_002480.3(PPP1R12A):c.2152C>T (p.Arg718Ter)	rs1034350880
NM_002480.3(PPP1R12A):c.3046G>A (p.Asp1016Asn)	rs2136954627
NM_002480.3(PPP1R12A):c.737A>C (p.Glu246Ala)

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