ClinVar Miner

List of variants in gene NCF2 reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 38
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000433.4(NCF2):c.257+273A>G rs789190 0.97340
NM_000433.4(NCF2):c.1000+295G>C rs4652813 0.87377
NM_000433.4(NCF2):c.366+261C>T rs699242 0.79036
NM_000433.4(NCF2):c.713+252T>C rs2236385 0.51034
NM_000433.4(NCF2):c.175-179T>C rs789192 0.49452
NM_000433.4(NCF2):c.542A>G (p.Lys181Arg) rs2274064 0.45656
NM_000433.4(NCF2):c.925-21G>A rs2296164 0.45071
NM_000433.4(NCF2):c.502-320C>A rs3818364 0.44976
NM_000433.4(NCF2):c.257+251G>A rs11578964 0.35149
NM_000433.4(NCF2):c.175-283A>G rs11588654 0.24470
NM_000433.4(NCF2):c.1291-246C>T rs9425306 0.23846
NM_000433.4(NCF2):c.174+186C>T rs10911365 0.19746
NM_000433.4(NCF2):c.1469-255T>A rs789180 0.17524
NM_000433.4(NCF2):c.258-2150T>C rs10911362 0.12365
NM_000433.4(NCF2):c.257+151C>T rs789191 0.11033
NM_000433.4(NCF2):c.174+295C>T rs34110768 0.09668
NM_000433.4(NCF2):c.258-190A>G rs10797888 0.08684
NM_000433.4(NCF2):c.366+232C>T rs699241 0.04122
NM_000433.4(NCF2):c.606G>A (p.Ala202=) rs17849501 0.03621
NM_000433.4(NCF2):c.1167C>A (p.His389Gln) rs17849502 0.03605
NM_000433.4(NCF2):c.1000+158C>A rs34823167 0.03379
NM_000433.4(NCF2):c.1290+130C>T rs3845461 0.03281
NM_000433.4(NCF2):c.855+78C>T rs6668645 0.01684
NM_000433.4(NCF2):c.890T>C (p.Val297Ala) rs35937854 0.01284
NM_000433.4(NCF2):c.1001-10T>G rs36113295 0.01255
NM_000433.4(NCF2):c.1256A>T (p.Asn419Ile) rs35012521 0.00520
NM_000433.4(NCF2):c.1360C>T (p.Pro454Ser) rs55761650 0.00401
NM_000433.4(NCF2):c.836C>T (p.Thr279Met) rs13306581 0.00088
NM_000433.4(NCF2):c.1179-4C>G rs55795842 0.00066
NM_000433.4(NCF2):c.1157G>A (p.Arg386Gln) rs147908264 0.00045
NM_000433.4(NCF2):c.1001-21C>T rs2102884171
NM_000433.4(NCF2):c.1183C>T (p.Arg395Trp) rs13306575
NM_000433.4(NCF2):c.1469-87A>C rs699244
NM_000433.4(NCF2):c.610-242del rs66977652
NM_000433.4(NCF2):c.610-296dup rs66625837
NM_000433.4(NCF2):c.714-114A>C rs2102891352
NM_000433.4(NCF2):c.714-116T>C rs2102891360
NM_000433.4(NCF2):c.924+250dup rs34708305

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.