List of variants in gene GFM1 reported as likely benign for not specified

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: 15

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_024996.7(GFM1):c.1990G>A (p.Val664Ile)	rs62288347	0.01504
NM_024996.7(GFM1):c.127A>G (p.Asn43Asp)	rs35942089	0.00900
NM_024996.7(GFM1):c.1764+11A>T	rs199739357	0.00265
NM_024996.7(GFM1):c.1324-15T>A	rs375168014	0.00057
NM_024996.7(GFM1):c.1032C>T (p.Asn344=)	rs373952002	0.00036
NM_024996.7(GFM1):c.597G>A (p.Ala199=)	rs148209578	0.00011
NM_024996.7(GFM1):c.1377C>T (p.Asn459=)	rs373098153	0.00004
NM_024996.7(GFM1):c.234+17G>A	rs532180547	0.00004
NM_024996.7(GFM1):c.1626A>G (p.Gln542=)	rs139042191	0.00002
NM_024996.7(GFM1):c.2071-20T>C	rs531105833	0.00001
NM_024996.7(GFM1):c.-25C>T	rs1057520288
NM_024996.7(GFM1):c.1909+13C>G	rs141146379
NM_024996.7(GFM1):c.1909+13C>T	rs141146379
NM_024996.7(GFM1):c.2125-11del	rs747030381
NM_024996.7(GFM1):c.2125-11dup	rs747030381

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.