List of variants in gene ELAC2 reported as benign for not specified

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_018127.7(ELAC2):c.1305-8T>C	rs3760316	0.32355
NM_018127.7(ELAC2):c.650C>T (p.Ser217Leu)	rs4792311	0.27559
NM_018127.7(ELAC2):c.297-11T>C	rs58809197	0.27292
NM_018127.7(ELAC2):c.1218+15C>T	rs55825263	0.26965
NM_018127.7(ELAC2):c.1304+17A>T	rs55674356	0.26960
NM_018127.7(ELAC2):c.1893A>G (p.Thr631=)	rs17552022	0.08581
NM_018127.7(ELAC2):c.491-14T>C	rs74556312	0.08556
NM_018127.7(ELAC2):c.798-20G>T	rs77528900	0.03735
NM_018127.7(ELAC2):c.1621G>A (p.Ala541Thr)	rs5030739	0.02886
NM_018127.7(ELAC2):c.2130C>T (p.Ser710=)	rs7217826	0.02093
NM_018127.7(ELAC2):c.1389C>T (p.Tyr463=)	rs77972324	0.01451
NM_018127.7(ELAC2):c.1479G>C (p.Pro493=)	rs140335642	0.00771
NM_018127.7(ELAC2):c.368-4T>A	rs139778647	0.00657
NM_018127.7(ELAC2):c.174G>A (p.Val58=)	rs2286334	0.00196
NM_018127.7(ELAC2):c.2108+14G>A	rs199942266	0.00004
NM_018127.7(ELAC2):c.1560A>G (p.Thr520=)	rs11545302
NM_018127.7(ELAC2):c.870+21_870+23dup	rs3217019

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