List of variants in gene ATP8B1 reported as benign 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: 22

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HGVS	dbSNP	gnomAD frequency
NM_001374385.1(ATP8B1):c.696T>C (p.Asp232=)	rs319438	0.99384
NM_001374385.1(ATP8B1):c.811A>C (p.Arg271=)	rs319443	0.99084
NM_001374385.1(ATP8B1):c.698+20C>T	rs319439	0.42536
NM_001374385.1(ATP8B1):c.3532-15C>T	rs12958967	0.19806
NM_001374385.1(ATP8B1):c.3531+8G>T	rs34027711	0.12129
NM_001374385.1(ATP8B1):c.2855G>A (p.Arg952Gln)	rs12968116	0.08072
NM_001374385.1(ATP8B1):c.3016-9C>A	rs34729241	0.01910
NM_001374385.1(ATP8B1):c.1739G>A (p.Ser580Asn)	rs33963153	0.01293
NM_001374385.1(ATP8B1):c.*11C>T	rs34255016	0.00974
NM_001374385.1(ATP8B1):c.2664G>T (p.Thr888=)	rs35757087	0.00529
NM_001374385.1(ATP8B1):c.2789G>A (p.Arg930Gln)	rs35623014	0.00451
NM_001374385.1(ATP8B1):c.1177A>G (p.Ile393Val)	rs34315917	0.00388
NM_001374385.1(ATP8B1):c.2442G>T (p.Lys814Asn)	rs34018300	0.00328
NM_001374385.1(ATP8B1):c.1286A>C (p.Glu429Ala)	rs34018205	0.00201
NM_001374385.1(ATP8B1):c.189A>G (p.Thr63=)	rs35377845	0.00198
NM_001374385.1(ATP8B1):c.3477C>T (p.Pro1159=)	rs117182648	0.00137
NM_001374385.1(ATP8B1):c.3744C>A (p.Thr1248=)	rs2271771	0.00137
NM_001374385.1(ATP8B1):c.1729A>G (p.Ile577Val)	rs3745078	0.00135
NM_001374385.1(ATP8B1):c.234C>G (p.His78Gln)	rs3745079	0.00124
NM_001374385.1(ATP8B1):c.2021T>C (p.Met674Thr)	rs35470719	0.00121
NM_001374385.1(ATP8B1):c.2931+14G>A	rs34451179	0.00101
NM_001374385.1(ATP8B1):c.3699G>A (p.Pro1233=)	rs35953143

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