List of variants in gene ELP1 reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_003640.5(ELP1):c.1965C>T (p.Thr655=)	rs2230791	0.09637
NM_003640.5(ELP1):c.1574G>A (p.Arg525Gln)	rs838827	0.07294
NM_003640.5(ELP1):c.934G>A (p.Glu312Lys)	rs1140064	0.02197
NM_003640.5(ELP1):c.959-15C>T	rs112114410	0.01906
NM_003640.5(ELP1):c.189C>T (p.Leu63=)	rs2230786	0.01873
NM_003640.5(ELP1):c.751A>G (p.Ser251Gly)	rs17853166	0.01640
NM_003640.5(ELP1):c.2587+14C>T	rs141670242	0.01614
NM_003640.5(ELP1):c.2855A>T (p.Lys952Ile)	rs2230798	0.01592
NM_003640.5(ELP1):c.3876T>G (p.Thr1292=)	rs61749202	0.01463
NM_003640.5(ELP1):c.1758T>G (p.Pro586=)	rs35054425	0.00792
NM_003640.5(ELP1):c.1230G>A (p.Pro410=)	rs41278359	0.00732
NM_003640.5(ELP1):c.1721C>T (p.Ala574Val)	rs35455790	0.00524
NM_003640.5(ELP1):c.2825G>A (p.Arg942Gln)	rs149845612

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