List of variants in gene SLC52A3 reported as benign for central nervous system disorder

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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: 28

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HGVS	dbSNP	gnomAD frequency
NM_033409.4(SLC52A3):c.1197+106A>G	rs6054589	0.85215
NM_033409.4(SLC52A3):c.568-200T>C	rs6133374	0.82884
NM_033409.4(SLC52A3):c.1233T>C (p.Ser411=)	rs910857	0.68551
NM_033409.4(SLC52A3):c.1197+108C>T	rs3746801	0.47446
NM_033409.4(SLC52A3):c.765C>T (p.Leu255=)	rs3746805	0.37656
NM_033409.4(SLC52A3):c.321C>T (p.Ala107=)	rs3746808	0.26517
NM_033409.4(SLC52A3):c.800C>T (p.Pro267Leu)	rs3746804	0.18642
NM_033409.4(SLC52A3):c.456C>T (p.Pro152=)	rs3746807	0.10172
NM_033409.4(SLC52A3):c.907A>G (p.Ile303Val)	rs3746802	0.09243
NM_033409.4(SLC52A3):c.222C>G (p.Ile74Met)	rs35655964	0.06422
NM_033409.4(SLC52A3):c.645C>T (p.Pro215=)	rs6054605	0.06184
NM_033409.4(SLC52A3):c.1048T>A (p.Leu350Met)	rs76947760	0.01629
NM_033409.4(SLC52A3):c.240C>T (p.Gly80=)	rs34376836	0.01265
NM_033409.4(SLC52A3):c.521A>G (p.Asp174Gly)	rs6054614	0.01033
NM_033409.4(SLC52A3):c.600C>T (p.Pro200=)	rs16992990	0.00815
NM_033409.4(SLC52A3):c.9C>T (p.Phe3=)	rs139486822	0.00809
NM_033409.4(SLC52A3):c.1047G>A (p.Ser349=)	rs147369439	0.00220
NM_033409.4(SLC52A3):c.981G>C (p.Leu327=)	rs62641669	0.00081
NM_033409.4(SLC52A3):c.936G>A (p.Ala312=)	rs6054602	0.00077
NM_033409.4(SLC52A3):c.339C>T (p.Phe113=)	rs151229044	0.00072
NM_033409.4(SLC52A3):c.363C>G (p.Thr121=)	rs749966154	0.00008
NM_033409.4(SLC52A3):c.-14_-6del	rs11467076
NM_033409.4(SLC52A3):c.1073+92T>C	rs8122335
NM_033409.4(SLC52A3):c.568-16_568-15insCTGATTGAC	rs3833341
NM_033409.4(SLC52A3):c.63T>C (p.Asn21=)	rs574008733
NM_033409.4(SLC52A3):c.705C>A (p.Leu235=)	rs3746806
NM_033409.4(SLC52A3):c.705C>T (p.Leu235=)	rs3746806
NM_033409.4(SLC52A3):c.833C>T (p.Thr278Met)	rs3746803

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