List of variants in gene JARID2 reported as benign by CeGaT Center for Human Genetics Tuebingen

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_004973.4(JARID2):c.1474C>T (p.Arg492Cys)	rs150448457	0.01001
NM_004973.4(JARID2):c.2230G>A (p.Asp744Asn)	rs142763537	0.00195
NM_004973.4(JARID2):c.2222C>T (p.Thr741Ile)	rs147485304	0.00144
NM_004973.4(JARID2):c.1459A>G (p.Lys487Glu)

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