List of variants in gene DHCR7 reported as likely 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: 45

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HGVS	dbSNP	gnomAD frequency
NM_001360.3(DHCR7):c.*119G>A	rs151230950	0.01111
NM_001360.3(DHCR7):c.98+88T>C	rs114935527	0.01079
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.627-71G>A	rs150290316	0.00652
NM_001360.3(DHCR7):c.*28G>T	rs114143715	0.00500
NM_001360.3(DHCR7):c.412+261G>A	rs190561005	0.00412
NM_001360.3(DHCR7):c.-6-108T>C	rs114439270	0.00364
NM_001360.3(DHCR7):c.626+67T>C	rs77184167	0.00361
NM_001360.3(DHCR7):c.98+205A>G	rs75644508	0.00359
NM_001360.3(DHCR7):c.322-229del	rs373799352	0.00331
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.208G>A (p.Gly70Ser)	rs144512551	0.00129
NM_001360.3(DHCR7):c.-6-119C>A	rs145746132	0.00100
NM_001360.3(DHCR7):c.199G>A (p.Ala67Thr)	rs143999854	0.00093
NM_001360.3(DHCR7):c.1012G>A (p.Val338Met)	rs72954276	0.00078
NM_001360.3(DHCR7):c.1368C>T (p.Gly456=)	rs144562471	0.00054
NM_001360.3(DHCR7):c.582C>T (p.Phe194=)	rs150603941	0.00038
NM_001360.3(DHCR7):c.927C>A (p.Gly309=)	rs149974099	0.00032
NM_001360.3(DHCR7):c.126C>T (p.Ser42=)	rs150928869	0.00031
NM_001360.3(DHCR7):c.139C>T (p.Leu47=)	rs140721259	0.00027
NM_001360.3(DHCR7):c.987C>T (p.Pro329=)	rs145901607	0.00024
NM_001360.3(DHCR7):c.729C>T (p.Pro243=)	rs145284180	0.00019
NM_001360.3(DHCR7):c.99-5C>T	rs372886043	0.00019
NM_001360.3(DHCR7):c.765C>T (p.Phe255=)	rs200132007	0.00011
NM_001360.3(DHCR7):c.1365C>T (p.Tyr455=)	rs557097410	0.00010
NM_001360.3(DHCR7):c.735C>T (p.Ile245=)	rs12800	0.00009
NM_001360.3(DHCR7):c.855C>T (p.Phe285=)	rs781026169	0.00007
NM_001360.3(DHCR7):c.522C>T (p.Phe174=)	rs140648594	0.00006
NM_001360.3(DHCR7):c.288C>T (p.Ala96=)	rs745595242	0.00005
NM_001360.3(DHCR7):c.69C>T (p.Thr23=)	rs199798127	0.00005
NM_001360.3(DHCR7):c.159C>T (p.Ile53=)	rs752952700	0.00004
NM_001360.3(DHCR7):c.507G>A (p.Ser169=)	rs138185442	0.00002
NM_001360.3(DHCR7):c.964-10C>T	rs753345689	0.00001
NM_001360.3(DHCR7):c.1143C>T (p.Ser381=)	rs1949270089
NM_001360.3(DHCR7):c.1350C>G (p.Arg450=)
NM_001360.3(DHCR7):c.1380G>A (p.Glu460=)
NM_001360.3(DHCR7):c.626+126_626+128del	rs145649767
NM_001360.3(DHCR7):c.70G>T (p.Ala24Ser)	rs146867923
NM_001360.3(DHCR7):c.906C>T (p.Phe302=)	rs80338858
NM_001360.3(DHCR7):c.963+30G>A
NM_001360.3(DHCR7):c.964-272_964-271dup	rs59663702
NM_001360.3(DHCR7):c.98+122del	rs112621523

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