List of variants in gene DHCR7 reported as likely benign by Fulgent Genetics, Fulgent Genetics

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: 18

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HGVS	dbSNP	gnomAD frequency
NM_001360.3(DHCR7):c.549C>T (p.Cys183=)	rs115446684	0.00470
NM_001360.3(DHCR7):c.1341C>T (p.Asp447=)	rs139721775	0.00296
NM_001360.3(DHCR7):c.208G>A (p.Gly70Ser)	rs144512551	0.00129
NM_001360.3(DHCR7):c.690G>C (p.Gly230=)	rs773393807	0.00009
NM_001360.3(DHCR7):c.303C>T (p.Thr101=)	rs777709295	0.00005
NM_001360.3(DHCR7):c.964-5C>T	rs767108226	0.00005
NM_001360.3(DHCR7):c.822C>T (p.Asn274=)	rs139787408	0.00003
NM_001360.3(DHCR7):c.279G>A (p.Thr93=)	rs774554996	0.00002
NM_001360.3(DHCR7):c.543G>C (p.Leu181=)	rs146839126	0.00002
NM_001360.3(DHCR7):c.342C>A (p.Leu114=)	rs773047702	0.00001
NM_001360.3(DHCR7):c.513C>T (p.Thr171=)	rs566499249	0.00001
NM_001360.3(DHCR7):c.964-10C>T	rs753345689	0.00001
NM_001360.3(DHCR7):c.99-7C>T	rs1177383343	0.00001
NM_001360.3(DHCR7):c.1098G>A (p.Gly366=)	rs2135939894
NM_001360.3(DHCR7):c.12A>G (p.Lys4=)	rs757934834
NM_001360.3(DHCR7):c.237T>C (p.His79=)	rs1316013264
NM_001360.3(DHCR7):c.304T>C (p.Leu102=)	rs1591113264
NM_001360.3(DHCR7):c.369C>T (p.Pro123=)	rs373452254

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