List of variants in gene DHCR7 reported as uncertain significance 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: 42

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HGVS	dbSNP	gnomAD frequency
NM_001360.3(DHCR7):c.400G>T (p.Val134Leu)	rs201466849	0.00041
NM_001360.3(DHCR7):c.988G>A (p.Val330Met)	rs139724817	0.00029
NM_001360.3(DHCR7):c.131T>C (p.Ile44Thr)	rs142897396	0.00019
NM_001360.3(DHCR7):c.719A>G (p.Asn240Ser)	rs148609143	0.00019
NM_001360.3(DHCR7):c.1088G>A (p.Arg363His)	rs200539324	0.00012
NM_001360.3(DHCR7):c.127G>A (p.Val43Ile)	rs200984695	0.00011
NM_001360.3(DHCR7):c.485C>T (p.Ala162Val)	rs398123606	0.00011
NM_001360.3(DHCR7):c.122C>T (p.Ala41Val)	rs761265690	0.00008
NM_001360.3(DHCR7):c.1354G>A (p.Ala452Thr)	rs140400648	0.00006
NM_001360.3(DHCR7):c.1406G>A (p.Arg469His)	rs201150384	0.00006
NM_001360.3(DHCR7):c.1099C>T (p.Arg367Cys)	rs531038145	0.00005
NM_001360.3(DHCR7):c.223A>T (p.Ile75Phe)	rs370748173	0.00005
NM_001360.3(DHCR7):c.418G>A (p.Val140Met)	rs373908315	0.00005
NM_001360.3(DHCR7):c.1087C>T (p.Arg363Cys)	rs547012639	0.00004
NM_001360.3(DHCR7):c.1091C>T (p.Thr364Met)	rs567600444	0.00004
NM_001360.3(DHCR7):c.1366G>A (p.Gly456Ser)	rs201847193	0.00004
NM_001360.3(DHCR7):c.770C>T (p.Ala257Val)	rs770925697	0.00004
NM_001360.3(DHCR7):c.1267G>A (p.Gly423Ser)	rs902179640	0.00003
NM_001360.3(DHCR7):c.289G>A (p.Ala97Thr)	rs150563256	0.00003
NM_001360.3(DHCR7):c.1159G>A (p.Gly387Arg)	rs765707139	0.00002
NM_001360.3(DHCR7):c.1231G>A (p.Asp411Asn)	rs372055524	0.00002
NM_001360.3(DHCR7):c.1369C>T (p.Arg457Trp)	rs371873032	0.00002
NM_001360.3(DHCR7):c.1370G>A (p.Arg457Gln)	rs886043122	0.00002
NM_001360.3(DHCR7):c.520T>G (p.Phe174Val)	rs886044698	0.00002
NM_001360.3(DHCR7):c.682C>T (p.Arg228Trp)	rs775773057	0.00002
NM_001360.3(DHCR7):c.1084C>T (p.Arg362Cys)	rs371302153	0.00001
NM_001360.3(DHCR7):c.1085G>A (p.Arg362His)	rs142213147	0.00001
NM_001360.3(DHCR7):c.1153G>A (p.Ala385Thr)	rs750989470	0.00001
NM_001360.3(DHCR7):c.1225G>A (p.Val409Ile)	rs757861528	0.00001
NM_001360.3(DHCR7):c.523G>A (p.Asp175Asn)	rs368269558	0.00001
NM_001360.3(DHCR7):c.616G>A (p.Ala206Thr)	rs542744675	0.00001
NM_001360.3(DHCR7):c.638G>A (p.Gly213Asp)	rs769583377	0.00001
NM_001360.3(DHCR7):c.658A>T (p.Met220Leu)	rs200659923	0.00001
NM_001360.3(DHCR7):c.823G>A (p.Val275Ile)	rs775628929	0.00001
NM_001360.3(DHCR7):c.947A>G (p.Tyr316Cys)	rs754992933	0.00001
NM_001360.3(DHCR7):c.956C>T (p.Thr319Met)	rs766583874	0.00001
NM_001360.3(DHCR7):c.1031G>A (p.Gly344Asp)	rs1409887214
NM_001360.3(DHCR7):c.1218C>G (p.Phe406Leu)	rs1949268068
NM_001360.3(DHCR7):c.1297A>G (p.Ile433Val)	rs1244124212
NM_001360.3(DHCR7):c.356A>G (p.His119Arg)	rs28938174
NM_001360.3(DHCR7):c.660G>C (p.Met220Ile)	rs767377692
NM_001360.3(DHCR7):c.70G>A (p.Ala24Thr)	rs146867923

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