List of variants in gene GFM1 reported as 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: 20

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HGVS	dbSNP	gnomAD frequency
NM_024996.7(GFM1):c.643G>A (p.Val215Ile)	rs2303909	0.58201
NM_024996.7(GFM1):c.18T>C (p.Ala6=)	rs1864507	0.58169
NM_024996.7(GFM1):c.*6C>T	rs1047355	0.42265
NM_024996.7(GFM1):c.-11C>T	rs112860155	0.01649
NM_024996.7(GFM1):c.1990G>A (p.Val664Ile)	rs62288347	0.01504
NM_024996.7(GFM1):c.476A>G (p.Asn159Ser)	rs34297061	0.01346
NM_024996.7(GFM1):c.1601+9G>C	rs77186707	0.01234
NM_024996.7(GFM1):c.1083+6T>G	rs142919829	0.00965
NM_024996.7(GFM1):c.127A>G (p.Asn43Asp)	rs35942089	0.00900
NM_024996.7(GFM1):c.1209C>T (p.Ala403=)	rs149949638	0.00899
NM_024996.7(GFM1):c.-31A>G	rs28372853	0.00742
NM_024996.7(GFM1):c.2071-17A>G	rs76679758	0.00671
NM_024996.7(GFM1):c.568A>C (p.Met190Leu)	rs75450876	0.00510
NM_024996.7(GFM1):c.368-18A>G	rs185654103	0.00478
NM_024996.7(GFM1):c.1593C>T (p.Ala531=)	rs114754676	0.00399
NM_024996.7(GFM1):c.960A>C (p.Pro320=)	rs145970222	0.00196
NM_024996.7(GFM1):c.690-5C>G	rs201685981	0.00124
NM_024996.7(GFM1):c.235-14G>A	rs201304690	0.00053
NM_024996.7(GFM1):c.-38C>T	rs377352238	0.00037
NM_024996.7(GFM1):c.77A>G (p.Lys26Arg)	rs574200635	0.00002

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