List of variants in gene EFHC1 reported as likely benign for not specified

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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: 23

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HGVS	dbSNP	gnomAD frequency
NM_018100.4(EFHC1):c.573+10A>G	rs9349626	0.18650
NM_018100.4(EFHC1):c.1343T>C (p.Met448Thr)	rs1266787	0.07947
NM_018100.4(EFHC1):c.1855A>C (p.Ile619Leu)	rs17851770	0.06310
NM_018100.4(EFHC1):c.545G>A (p.Arg182His)	rs3804505	0.05453
NM_018100.4(EFHC1):c.881G>A (p.Arg294His)	rs1570624	0.00969
NM_018100.4(EFHC1):c.229C>A (p.Pro77Thr)	rs149055334	0.00789
NM_018100.4(EFHC1):c.662G>A (p.Arg221His)	rs79761183	0.00778
NM_018100.4(EFHC1):c.1224C>T (p.Asp408=)	rs116134831	0.00613
NM_018100.4(EFHC1):c.25T>C (p.Leu9=)	rs149315015	0.00264
NM_018100.4(EFHC1):c.685T>C (p.Phe229Leu)	rs137852776	0.00242
NM_018100.4(EFHC1):c.1155C>T (p.Asn385=)	rs115913738	0.00210
NM_018100.4(EFHC1):c.64-5T>C	rs201860746	0.00063
NM_018100.4(EFHC1):c.1675T>C (p.Leu559=)	rs145194882	0.00024
NM_018100.4(EFHC1):c.661C>T (p.Arg221Cys)	rs139197513	0.00019
NM_018100.4(EFHC1):c.779G>A (p.Arg260Gln)	rs145754721	0.00008
NM_018100.4(EFHC1):c.1584C>T (p.Leu528=)	rs774640110	0.00006
NM_018100.4(EFHC1):c.1812A>C (p.Glu604Asp)	rs369503191	0.00006
NM_018100.4(EFHC1):c.627T>C (p.Leu209=)	rs141142186	0.00003
NM_018100.4(EFHC1):c.43A>G (p.Thr15Ala)	rs750899949	0.00002
NM_018100.4(EFHC1):c.1278+15T>C	rs376515287	0.00001
NM_018100.4(EFHC1):c.547G>A (p.Val183Ile)	rs769591944	0.00001
NM_018100.4(EFHC1):c.-13G>A	rs1057520834
NM_018100.4(EFHC1):c.475C>T (p.Arg159Trp)	rs3804506

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