List of variants in gene ABCB6 reported by Mayo Clinic Laboratories, Mayo Clinic

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_005689.4(ABCB6):c.1361T>C (p.Val454Ala)	rs61733629	0.00285
NM_005689.4(ABCB6):c.1943G>A (p.Arg648Gln)	rs13402964	0.00182
NM_005689.4(ABCB6):c.2168G>A (p.Arg723Gln)	rs148211042	0.00073
NM_005689.4(ABCB6):c.2041G>A (p.Ala681Thr)	rs142421126	0.00041
NM_005689.4(ABCB6):c.2215C>T (p.Arg739Cys)	rs141840760	0.00028
NM_005689.4(ABCB6):c.2216G>A (p.Arg739His)	rs192931087	0.00022
NM_005689.4(ABCB6):c.1402G>T (p.Ala468Ser)	rs777270402	0.00005
NM_005689.4(ABCB6):c.2063G>A (p.Arg688His)	rs757264353	0.00004
NM_005689.4(ABCB6):c.2465G>T (p.Trp822Leu)	rs754250687	0.00002
NM_005689.4(ABCB6):c.1979C>A (p.Ala660Asp)	rs140239756
NM_005689.4(ABCB6):c.1979C>T (p.Ala660Val)	rs140239756
NM_005689.4(ABCB6):c.2420+1G>A
NM_005689.4(ABCB6):c.2512C>T (p.Gln838Ter)
NM_005689.4(ABCB6):c.803G>T (p.Cys268Phe)
NM_005689.4(ABCB6):c.827G>C (p.Arg276Pro)

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