List of variants in gene PRSS12 reported as likely benign for autosomal recessive disease

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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: 11

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HGVS	dbSNP	gnomAD frequency
NM_003619.4(PRSS12):c.*1504G>A	rs1045817	0.11039
NM_003619.4(PRSS12):c.*807G>A	rs17516164	0.06563
NM_003619.4(PRSS12):c.*208C>T	rs142775631	0.01464
NM_003619.4(PRSS12):c.1773C>T (p.His591=)	rs34131974	0.00712
NM_003619.4(PRSS12):c.51A>G (p.Glu17=)	rs144853134	0.00447
NM_003619.4(PRSS12):c.2389C>T (p.Arg797Cys)	rs35996030	0.00375
NM_003619.4(PRSS12):c.523G>A (p.Gly175Ser)	rs145151396	0.00273
NM_003619.4(PRSS12):c.440C>T (p.Pro147Leu)	rs72903215	0.00212
NM_003619.4(PRSS12):c.*764A>G	rs11098431	0.00041
NM_003619.4(PRSS12):c.*1865T>C	rs183712097	0.00023
NM_003619.4(PRSS12):c.-10C>T	rs559605488	0.00001

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