List of variants in gene ERLIN2 reported by Genetic Services Laboratory, University of Chicago

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_007175.8(ERLIN2):c.318C>T (p.Asn106=)	rs16887018	0.02374
NM_007175.8(ERLIN2):c.696G>A (p.Lys232=)	rs138164407	0.00313
NM_007175.8(ERLIN2):c.123G>A (p.Leu41=)	rs112575270	0.00103
NM_007175.8(ERLIN2):c.819+3A>G	rs377704533	0.00013
NM_007175.8(ERLIN2):c.384C>T (p.Cys128=)	rs200292614	0.00007
NM_007175.8(ERLIN2):c.219T>C (p.Asn73=)	rs377044758	0.00006
NM_007175.8(ERLIN2):c.589G>A (p.Ala197Thr)	rs149254654	0.00001
NM_007175.8(ERLIN2):c.1002_1007del (p.Ala335_Thr336del)	rs797045563
NM_007175.8(ERLIN2):c.299-4_299-3del	rs778852699
NM_007175.8(ERLIN2):c.557_557+10delinsCCTGGCTGTGACCTGGGCTGTGA	rs1554517382
NM_007175.8(ERLIN2):c.740-5C>G	rs191003311

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