List of variants in gene SLC4A1 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000342.4(SLC4A1):c.702C>T (p.Ala234=)	rs188161190	0.00153
NM_000342.4(SLC4A1):c.615T>C (p.Asp205=)	rs5038	0.00070
NM_000342.4(SLC4A1):c.-3G>A	rs372104017	0.00015
NM_000342.4(SLC4A1):c.1224C>T (p.Ala408=)	rs142226515	0.00002
NM_000342.4(SLC4A1):c.2184C>T (p.Thr728=)	rs150858709	0.00002
NM_000342.4(SLC4A1):c.1242T>C (p.Phe414=)	rs2144614043

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