List of variants in gene FECH reported as benign for not provided

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: 38

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HGVS	dbSNP	gnomAD frequency
NM_000140.5(FECH):c.314+23A>G	rs577152	0.98504
NM_000140.5(FECH):c.921A>G (p.Pro307=)	rs536560	0.74784
NM_000140.5(FECH):c.705+211A>G	rs1736439	0.59106
NM_000140.5(FECH):c.804+123A>G	rs1736440	0.59036
NM_000140.5(FECH):c.599-255G>A	rs3817726	0.58495
NM_000140.5(FECH):c.706-198T>C	rs1646594	0.52341
NM_000140.5(FECH):c.315-279T>G	rs71355627	0.26978
NM_000140.5(FECH):c.*248C>T	rs8339	0.21849
NM_000140.5(FECH):c.912+94T>A	rs28617328	0.15827
NM_000140.5(FECH):c.195-111A>G	rs35655063	0.14186
NM_000140.5(FECH):c.194+187G>A	rs71355630	0.11943
NM_000140.5(FECH):c.287G>A (p.Arg96Gln)	rs1041951	0.10933
NM_000140.5(FECH):c.1138-61G>A	rs12957678	0.10159
NM_000140.5(FECH):c.1077+117_1077+123del	rs58628398	0.10154
NM_000140.5(FECH):c.913-62_913-61del	rs60626363	0.10134
NM_000140.5(FECH):c.804+263A>G	rs9956673	0.10093
NM_000140.5(FECH):c.464-299A>T	rs58442256	0.09634
NM_000140.5(FECH):c.598+301G>A	rs2269222	0.08954
NM_000140.5(FECH):c.1077+252T>C	rs72627248	0.08211
NM_000140.5(FECH):c.913-43A>C	rs28451199	0.04371
NM_000140.5(FECH):c.599-112C>G	rs9963013	0.04274
NM_000140.5(FECH):c.194+306C>T	rs73436947	0.03650
NM_000140.5(FECH):c.804+279T>C	rs111761849	0.03163
NM_000140.5(FECH):c.194+43C>T	rs61202988	0.02500
NM_000140.5(FECH):c.463+43C>T	rs73959100	0.00654
NM_000140.5(FECH):c.1077+35C>T	rs77695117	0.00243
NM_000140.5(FECH):c.183A>G (p.Gln61=)	rs76286732	0.00177
NM_000140.5(FECH):c.705+19G>C	rs202119041	0.00176
NM_000140.5(FECH):c.514G>A (p.Glu172Lys)	rs200650502	0.00001
NM_000140.5(FECH):c.1078-51del	rs57800921
NM_000140.5(FECH):c.163G>A (p.Gly55Ser)	rs3848519
NM_000140.5(FECH):c.163G>T (p.Gly55Cys)	rs3848519
NM_000140.5(FECH):c.291C>T (p.Asp97=)	rs577947755
NM_000140.5(FECH):c.384C>T (p.Gly128=)
NM_000140.5(FECH):c.798C>G (p.Pro266=)	rs536765
NM_000140.5(FECH):c.804+217dup	rs3216687
NM_000140.5(FECH):c.913-7C>T	rs369538477
NM_000140.5(FECH):c.949G>A (p.Glu317Lys)

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