List of variants in gene DGAT1 reported as benign for not provided

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: 27

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HGVS	dbSNP	gnomAD frequency
NM_012079.6(DGAT1):c.288+264C>T	rs3890400	0.32531
NM_012079.6(DGAT1):c.468+46C>T	rs141056262	0.08122
NM_012079.6(DGAT1):c.743C>A (p.Thr248Asn)	rs55962377	0.06259
NM_012079.6(DGAT1):c.579C>T (p.Gly193=)	rs56180335	0.04745
NM_012079.6(DGAT1):c.330-14C>A	rs56126815	0.02450
NM_012079.6(DGAT1):c.455A>G (p.Lys152Arg)	rs55907012	0.01307
NM_012079.6(DGAT1):c.1401A>T (p.Ile467=)	rs148218968	0.00523
NM_012079.6(DGAT1):c.677-4G>A	rs200950681	0.00520
NM_012079.6(DGAT1):c.1335C>T (p.Gly445=)	rs146197651	0.00475
NM_012079.6(DGAT1):c.465G>A (p.Ala155=)	rs142990281	0.00240
NM_012079.6(DGAT1):c.797A>G (p.Asn266Ser)	rs146196839	0.00151
NM_012079.6(DGAT1):c.1407C>T (p.Val469=)	rs17851331	0.00139
NM_012079.6(DGAT1):c.432T>C (p.Ala144=)	rs148532878	0.00079
NM_012079.6(DGAT1):c.1454C>T (p.Ala485Val)	rs200430497	0.00066
NM_012079.6(DGAT1):c.789C>T (p.Tyr263=)	rs149913927	0.00046
NM_012079.6(DGAT1):c.200+18C>T	rs989432463	0.00016
NM_012079.6(DGAT1):c.1161-12C>T	rs782529920	0.00003
NM_012079.6(DGAT1):c.792G>A (p.Glu264=)	rs139081729	0.00003
NM_012079.6(DGAT1):c.1422C>T (p.His474=)	rs564805332	0.00001
NM_012079.6(DGAT1):c.1160+10dup
NM_012079.6(DGAT1):c.1248+17dup
NM_012079.6(DGAT1):c.330-3del
NM_012079.6(DGAT1):c.574+10dup
NM_012079.6(DGAT1):c.752-14del
NM_012079.6(DGAT1):c.856-3C>T	rs201711241
NM_012079.6(DGAT1):c.856-3del	rs781961359
NM_012079.6(DGAT1):c.856-3dup	rs781961359

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