List of variants in gene SLC9A3 reported 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
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_004174.4(SLC9A3):c.1233C>T (p.Tyr411=)	rs143144929	0.00417
NM_004174.4(SLC9A3):c.2158A>G (p.Thr720Ala)	rs145183553	0.00162
NM_004174.4(SLC9A3):c.1832C>T (p.Ala611Val)	rs145635595	0.00075
NM_004174.4(SLC9A3):c.312C>T (p.His104=)	rs142857053	0.00022
NM_004174.4(SLC9A3):c.1143C>T (p.Tyr381=)	rs375272660	0.00016
NM_004174.4(SLC9A3):c.1509C>G (p.Leu503=)	rs371452813	0.00004
NM_004174.4(SLC9A3):c.1848G>A (p.Thr616=)	rs368902663	0.00002
NM_004174.4(SLC9A3):c.1518-3C>T	rs369382043	0.00001
NM_004174.4(SLC9A3):c.805G>A (p.Ala269Thr)	rs869312807	0.00001
NM_004174.4(SLC9A3):c.*235G>T	rs866897416
NM_004174.4(SLC9A3):c.*88G>C	rs540024518
NM_004174.4(SLC9A3):c.1557C>T (p.Leu519=)	rs2477568439

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