List of variants in gene CACNA1H reported as uncertain significance for not specified

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_021098.3(CACNA1H):c.4120G>A (p.Val1374Met)	rs201855332	0.00018
NM_021098.3(CACNA1H):c.2542G>A (p.Gly848Ser)	rs374272094	0.00017
NM_021098.3(CACNA1H):c.6023G>T (p.Ser2008Ile)	rs750277154	0.00009
NM_021098.3(CACNA1H):c.4567-4A>G	rs1055632728	0.00006
NM_021098.3(CACNA1H):c.2990C>T (p.Ala997Val)	rs375023370	0.00004
NM_021098.3(CACNA1H):c.4736G>A (p.Arg1579Gln)	rs367947771	0.00004
NM_021098.3(CACNA1H):c.2071G>A (p.Gly691Ser)	rs377664706	0.00002
NM_021098.3(CACNA1H):c.2907+10G>A	rs781264742	0.00002
NM_021098.3(CACNA1H):c.3698A>T (p.Asp1233Val)	rs774604155	0.00001
NM_021098.3(CACNA1H):c.1516C>G (p.Arg506Gly)	rs58593315
NM_021098.3(CACNA1H):c.1918C>G (p.Pro640Ala)
NM_021098.3(CACNA1H):c.2360G>A (p.Arg787His)
NM_021098.3(CACNA1H):c.280C>G (p.Leu94Val)
NM_021098.3(CACNA1H):c.3466C>T (p.Arg1156Cys)
NM_021098.3(CACNA1H):c.3920A>G (p.Asn1307Ser)	rs767633946
NM_021098.3(CACNA1H):c.4754G>T (p.Arg1585Leu)	rs774569737
NM_021098.3(CACNA1H):c.5206C>T (p.Arg1736Cys)	rs750143885
NM_021098.3(CACNA1H):c.770G>A (p.Arg257Gln)

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