List of variants in gene ABCB11 reported as benign by Eurofins NTD LLC (GA)

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_003742.4(ABCB11):c.1331T>C (p.Val444Ala)	rs2287622	0.57004
NM_003742.4(ABCB11):c.3084A>G (p.Ala1028=)	rs497692	0.46166
NM_003742.4(ABCB11):c.2093G>A (p.Arg698His)	rs138642043	0.00495
NM_003742.4(ABCB11):c.2134T>C (p.Leu712=)	rs191649793	0.00401
NM_003742.4(ABCB11):c.616A>G (p.Ile206Val)	rs11568357	0.00297
NM_003742.4(ABCB11):c.2943C>T (p.Tyr981=)	rs145720664	0.00273
NM_003742.4(ABCB11):c.1791G>T (p.Val597=)	rs11568371	0.00145
NM_003742.4(ABCB11):c.2101T>C (p.Ser701Pro)	rs150572999	0.00079
NM_003742.4(ABCB11):c.1772A>G (p.Asn591Ser)	rs11568367	0.00054
NM_003742.4(ABCB11):c.1605C>T (p.Ala535=)	rs144848376	0.00039
NM_003742.4(ABCB11):c.2594C>T (p.Ala865Val)	rs118109635	0.00029
NM_003742.4(ABCB11):c.399C>T (p.Asn133=)	rs537575091
NM_003742.4(ABCB11):c.957A>G (p.Gly319=)	rs7563233

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