List of variants in gene SLCO5A1 reported as benign for not provided

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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: 26

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HGVS	dbSNP	gnomAD frequency
NM_030958.3(SLCO5A1):c.1424-104C>T	rs2959578	0.70981
NM_030958.3(SLCO5A1):c.97C>T (p.Leu33Phe)	rs3750266	0.49948
NM_030958.3(SLCO5A1):c.-263G>T	rs3750268	0.29777
NM_030958.3(SLCO5A1):c.2024+301A>C	rs4737288	0.20085
NM_030958.3(SLCO5A1):c.762C>T (p.Asp254=)	rs35318751	0.01782
NM_030958.3(SLCO5A1):c.311C>G (p.Thr104Ser)	rs35616937	0.01391
NM_030958.3(SLCO5A1):c.2352G>A (p.Val784=)	rs61733912	0.00937
NM_030958.3(SLCO5A1):c.1781G>T (p.Gly594Val)	rs34698405	0.00921
NM_030958.3(SLCO5A1):c.2328C>G (p.Pro776=)	rs80078382	0.00497
NM_030958.3(SLCO5A1):c.53C>T (p.Pro18Leu)	rs61730155	0.00471
NM_030958.3(SLCO5A1):c.1124G>A (p.Arg375Gln)	rs149362749	0.00406
NM_030958.3(SLCO5A1):c.954A>G (p.Leu318=)	rs142227692	0.00396
NM_030958.3(SLCO5A1):c.1215G>A (p.Ala405=)	rs34295070	0.00360
NM_030958.3(SLCO5A1):c.742C>T (p.Pro248Ser)	rs118016633	0.00309
NM_030958.3(SLCO5A1):c.255C>T (p.Ala85=)	rs141633279	0.00228
NM_030958.3(SLCO5A1):c.2024+17A>G	rs142085897	0.00183
NM_030958.3(SLCO5A1):c.2428C>T (p.Leu810=)	rs150778647	0.00154
NM_030958.3(SLCO5A1):c.2025-20C>T	rs142637717	0.00151
NM_030958.3(SLCO5A1):c.276C>T (p.Leu92=)	rs142293423	0.00140
NM_030958.3(SLCO5A1):c.2326C>T (p.Pro776Ser)	rs117676215	0.00059
NM_030958.3(SLCO5A1):c.1464C>T (p.Leu488=)	rs200618319	0.00024
NM_030958.3(SLCO5A1):c.907+10T>G	rs142257390	0.00023
NM_030958.3(SLCO5A1):c.327C>T (p.Ser109=)	rs145247874	0.00011
NM_030958.3(SLCO5A1):c.2310G>A (p.Arg770=)	rs542918610	0.00001
NM_030958.3(SLCO5A1):c.2472C>T (p.Pro824=)	rs528114944	0.00001
NM_030958.3(SLCO5A1):c.2055A>G (p.Ala685=)	rs10448034

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