List of variants in gene IMPG2 reported as likely 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_016247.4(IMPG2):c.*685A>G	rs537248333	0.00293
NM_016247.4(IMPG2):c.3038C>T (p.Pro1013Leu)	rs116450347	0.00272
NM_016247.4(IMPG2):c.1223C>T (p.Thr408Met)	rs148056371	0.00032
NM_016247.4(IMPG2):c.1224G>A (p.Thr408=)	rs113384204	0.00006
NM_016247.4(IMPG2):c.*690TA[5]
NM_016247.4(IMPG2):c.2892A>G (p.Arg964=)
NM_016247.4(IMPG2):c.534-13dup	rs567795716
NM_016247.4(IMPG2):c.534-5del

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