List of variants in gene BICD2 reported as benign by GeneDx

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: 23

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001003800.2(BICD2):c.1063-111G>C	rs56339669	0.26288
NM_001003800.2(BICD2):c.453+212A>G	rs2296080	0.26205
NM_001003800.2(BICD2):c.2259-206C>A	rs10992430	0.26148
NM_001003800.2(BICD2):c.240+120C>G	rs2277164	0.26013
NM_001003800.2(BICD2):c.*1499C>T	rs3739605	0.17864
NM_001003800.2(BICD2):c.1063-130G>A	rs12238691	0.17359
NM_001003800.2(BICD2):c.240+102C>T	rs116966595	0.07899
NM_001003800.2(BICD2):c.*1789C>A	rs10992429	0.06028
NM_001003800.2(BICD2):c.607-161T>C	rs12236118	0.04088
NM_001003800.2(BICD2):c.1062+46C>G	rs41273374	0.03700
NM_001003800.2(BICD2):c.2107-21C>T	rs79574551	0.03009
NM_001003800.2(BICD2):c.269A>G (p.Lys90Arg)	rs61754130	0.00437
NM_001003800.2(BICD2):c.2445G>A (p.Pro815=)	rs34451610	0.00337
NM_001003800.2(BICD2):c.1806G>A (p.Thr602=)	rs138300993	0.00118
NM_001003800.2(BICD2):c.1179T>A (p.Asn393Lys)	rs144427583	0.00066
NM_001003800.2(BICD2):c.2397C>T (p.Leu799=)	rs151133287	0.00061
NM_001003800.2(BICD2):c.1050G>A (p.Gln350=)	rs368860496	0.00044
NM_001003800.2(BICD2):c.753C>T (p.Arg251=)	rs533852054	0.00010
NM_001003800.2(BICD2):c.2350A>G (p.Met784Val)	rs149891938	0.00008
NM_001003800.2(BICD2):c.1725C>G (p.Pro575=)	rs201343832	0.00003
NM_001003800.2(BICD2):c.1376C>T (p.Thr459Met)	rs777065935	0.00001
NM_001003800.2(BICD2):c.1697G>T (p.Arg566Leu)	rs550312355
NM_001003800.2(BICD2):c.454-234_454-233insGTGTCAG	rs61259632

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.