Variants in gene ABCG8 with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 14

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HGVS	dbSNP	gnomAD frequency
NM_022437.3(ABCG8):c.1201A>T (p.Thr401Ser)	rs144200355	0.00179
NM_022437.3(ABCG8):c.1785C>T (p.Phe595=)	rs139677898	0.00123
NM_022437.3(ABCG8):c.1645G>A (p.Ala549Thr)	rs140690030	0.00103
NM_022437.3(ABCG8):c.1924G>A (p.Ala642Thr)	rs113005049	0.00096
NM_022437.3(ABCG8):c.1941C>G (p.Val647=)	rs147991100	0.00094
NM_022437.3(ABCG8):c.1093A>G (p.Thr365Ala)	rs114404835	0.00093
NM_022437.3(ABCG8):c.1411+8T>A	rs201991639	0.00078
NM_022437.3(ABCG8):c.322+6G>A	rs181319879	0.00022
NM_022437.3(ABCG8):c.1212-7T>A	rs759300542	0.00011
NM_022437.3(ABCG8):c.870C>T (p.Thr290=)	rs117221284	0.00009
NM_022437.3(ABCG8):c.1667T>C (p.Phe556Ser)	rs548098742	0.00002
NM_022437.3(ABCG8):c.1117T>C (p.Cys373Arg)	rs554680915	0.00001
NM_022437.3(ABCG8):c.1285A>G (p.Met429Val)	rs147194762
NM_022437.3(ABCG8):c.1756+16G>A

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