List of variants in gene XIRP2 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_152381.6(XIRP2):c.5069C>T (p.Thr1690Ile)	rs184983098	0.00262
NM_152381.6(XIRP2):c.3954C>G (p.Thr1318=)	rs149234026	0.00179
NM_152381.6(XIRP2):c.9126G>A (p.Pro3042=)	rs191522105	0.00148
NM_152381.6(XIRP2):c.8224A>G (p.Thr2742Ala)	rs202045863	0.00118
NM_152381.6(XIRP2):c.*1241T>C
NM_152381.6(XIRP2):c.21C>T (p.Gly7=)
NM_152381.6(XIRP2):c.4128AGA[1] (p.Glu1377del)
NM_152381.6(XIRP2):c.7094C>T (p.Pro2365Leu)
NM_152381.6(XIRP2):c.7269A>G (p.Thr2423=)

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