List of variants in gene DNAJC12 reported as benign by GeneDx

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_021800.3(DNAJC12):c.79-269C>T	rs4540739	0.99962
NM_021800.3(DNAJC12):c.79-56C>T	rs962608	0.73059
NM_021800.3(DNAJC12):c.503-277T>C	rs7101093	0.16475
NM_021800.3(DNAJC12):c.243C>T (p.Ser81=)	rs3740049	0.13116
NC_000010.11:g.67838376T>C	rs112750745	0.09134
NM_021800.3(DNAJC12):c.79-250T>C	rs117850520	0.08952
NM_021800.3(DNAJC12):c.-17C>T	rs2273771	0.07185
NM_021800.3(DNAJC12):c.*142A>G	rs41299238	0.05197
NM_021800.3(DNAJC12):c.297+18T>G	rs77068920	0.02971
NM_021800.3(DNAJC12):c.502+51T>C	rs77971812	0.02468
NM_021800.3(DNAJC12):c.387T>G (p.Cys129Trp)	rs36099123	0.02463
NM_021800.3(DNAJC12):c.502+114T>C	rs78162003	0.02460
NM_021800.3(DNAJC12):c.372G>T (p.Met124Ile)	rs35690028	0.02289
NM_021800.3(DNAJC12):c.502+132A>G	rs75094170	0.02287
NM_021800.3(DNAJC12):c.157+135A>G	rs75536697	0.02081
NM_021800.3(DNAJC12):c.*72T>C	rs79297589	0.01755
NM_021800.3(DNAJC12):c.298-266G>A	rs73271977	0.01555

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