List of variants in gene GFM1 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_024996.7(GFM1):c.788A>G (p.Gln263Arg)	rs115984741	0.00158
NM_024996.7(GFM1):c.690-5C>G	rs201685981	0.00124
NM_024996.7(GFM1):c.1343A>G (p.Asp448Gly)	rs146951325	0.00080
NM_024996.7(GFM1):c.1032C>T (p.Asn344=)	rs373952002	0.00036
NM_024996.7(GFM1):c.88T>G (p.Trp30Gly)	rs760733794	0.00006
NM_024996.7(GFM1):c.1311C>T (p.Ser437=)	rs199976566	0.00005
NM_024996.7(GFM1):c.1377C>T (p.Asn459=)	rs373098153	0.00004
NM_024996.7(GFM1):c.1704A>G (p.Glu568=)	rs756847811	0.00003

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