List of variants in gene DNAJC21 reported as uncertain significance for immune system disorder

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001012339.3(DNAJC21):c.1024G>A (p.Val342Met)	rs144600070	0.00471
NM_001012339.3(DNAJC21):c.1186-531G>A	rs112971776	0.00144
NM_001012339.3(DNAJC21):c.191+10A>G	rs368399096	0.00102
NM_001012339.3(DNAJC21):c.958G>A (p.Asp320Asn)	rs148374246	0.00058
NM_001012339.3(DNAJC21):c.1481G>A (p.Arg494Gln)	rs146933471	0.00050
NM_001012339.3(DNAJC21):c.410T>C (p.Phe137Ser)	rs752188838	0.00001
NM_001012339.3(DNAJC21):c.1015C>T (p.Arg339Trp)	rs368712421
NM_001012339.3(DNAJC21):c.1016G>A (p.Arg339Gln)	rs142389949
NM_001012339.3(DNAJC21):c.1368del (p.Lys456fs)	rs756768331
NM_001012339.3(DNAJC21):c.203A>G (p.His68Arg)
NM_001012339.3(DNAJC21):c.463T>C (p.Trp155Arg)	rs1580526653

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