Variants in gene GFM1 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 19

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HGVS	dbSNP	gnomAD frequency
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.1601+9G>C	rs77186707	0.01234
NM_024996.7(GFM1):c.127A>G (p.Asn43Asp)	rs35942089	0.00900
NM_024996.7(GFM1):c.568A>C (p.Met190Leu)	rs75450876	0.00510
NM_024996.7(GFM1):c.1593C>T (p.Ala531=)	rs114754676	0.00399
NM_024996.7(GFM1):c.1764+11A>T	rs199739357	0.00265
NM_024996.7(GFM1):c.2190C>T (p.Asp730=)	rs149049400	0.00196
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.1324-15T>A	rs375168014	0.00057
NM_024996.7(GFM1):c.-38C>T	rs377352238	0.00037
NM_024996.7(GFM1):c.1032C>T (p.Asn344=)	rs373952002	0.00036
NM_024996.7(GFM1):c.2059C>T (p.Leu687=)	rs771619705	0.00007
NM_024996.7(GFM1):c.2071-20T>C	rs531105833	0.00001
NM_024996.7(GFM1):c.1909+13C>G	rs141146379
NM_024996.7(GFM1):c.1909+13C>T	rs141146379
NM_024996.7(GFM1):c.2125-11dup	rs747030381
NM_024996.7(GFM1):c.56C>T (p.Ala19Val)	rs567086019

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