Variants in gene DHCR7 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) 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: 17

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HGVS	dbSNP	gnomAD frequency
NM_001360.3(DHCR7):c.*119G>A	rs151230950	0.01111
NM_001360.3(DHCR7):c.570C>T (p.Ala190=)	rs74909468	0.01097
NM_001360.3(DHCR7):c.25A>T (p.Ile9Phe)	rs115595829	0.00983
NM_001360.3(DHCR7):c.-195G>T	rs141057811	0.00755
NM_001360.3(DHCR7):c.99-10G>A	rs189549129	0.00495
NM_001360.3(DHCR7):c.549C>T (p.Cys183=)	rs115446684	0.00470
NM_001360.3(DHCR7):c.1008C>T (p.His336=)	rs75225632	0.00447
NM_001360.3(DHCR7):c.1341C>T (p.Asp447=)	rs139721775	0.00296
NM_001360.3(DHCR7):c.399C>T (p.Ala133=)	rs147424205	0.00248
NM_001360.3(DHCR7):c.321+10C>T	rs377108406	0.00189
NM_001360.3(DHCR7):c.1012G>A (p.Val338Met)	rs72954276	0.00078
NM_001360.3(DHCR7):c.126C>T (p.Ser42=)	rs150928869	0.00031
NM_001360.3(DHCR7):c.586A>G (p.Met196Val)	rs200474791	0.00026
NM_001360.3(DHCR7):c.987C>T (p.Pro329=)	rs145901607	0.00024
NM_001360.3(DHCR7):c.226G>A (p.Val76Ile)	rs368473756	0.00001
NM_001360.3(DHCR7):c.161_172del	rs141483210
NM_001360.3(DHCR7):c.70G>T (p.Ala24Ser)	rs146867923

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