List of variants reported as likely benign for basal ganglia calcification, idiopathic, 1 by Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001257180.2(SLC20A2):c.1812C>T (p.Ala604=)	rs116401889	0.00456
NM_001257180.2(SLC20A2):c.345G>A (p.Thr115=)	rs34124953	0.00417
NM_001257180.2(SLC20A2):c.933C>T (p.Tyr311=)	rs115902470	0.00289
NM_001257180.2(SLC20A2):c.58T>C (p.Leu20=)	rs115993270	0.00262

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