List of variants in gene combination EDAR, RANBP2 reported as likely benign by Illumina Laboratory Services, Illumina

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: 25

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HGVS	dbSNP	gnomAD frequency
NM_022336.4(EDAR):c.*935C>T	rs3749096	0.14095
NM_022336.4(EDAR):c.*757T>C	rs3749097	0.08815
NM_022336.4(EDAR):c.357-4G>A	rs748225	0.07354
NM_022336.4(EDAR):c.*1248G>T	rs75155869	0.05209
NM_022336.4(EDAR):c.*1900C>T	rs200762071	0.03161
NM_022336.4(EDAR):c.*895C>T	rs115259025	0.02162
NM_022336.4(EDAR):c.*999C>T	rs10206737	0.02037
NM_022336.4(EDAR):c.*328G>A	rs75703116	0.01927
NM_022336.4(EDAR):c.*1107C>T	rs73952545	0.01003
NM_022336.4(EDAR):c.*1366A>G	rs187951842	0.00322
NM_022336.4(EDAR):c.319A>G (p.Met107Val)	rs61761321	0.00302
NM_022336.4(EDAR):c.*1364T>G	rs147757790	0.00105
NM_022336.4(EDAR):c.731-4G>T	rs201539805	0.00035
NM_022336.4(EDAR):c.68C>T (p.Ser23Leu)	rs760731007	0.00014
NM_022336.4(EDAR):c.224C>T (p.Pro75Leu)	rs748806220	0.00006
NM_022336.4(EDAR):c.675G>A (p.Pro225=)	rs746044070	0.00005
NM_022336.4(EDAR):c.156G>A (p.Pro52=)	rs3749101	0.00004
NM_022336.4(EDAR):c.463G>A (p.Ala155Thr)	rs370972367	0.00004
NM_022336.3(EDAR):c.*2450G>A	rs17037035
NM_022336.4(EDAR):c.*1888GAGT[1]	rs145115545
NM_022336.4(EDAR):c.2151_2154dup	rs111463955
NM_022336.4(EDAR):c.1017C>T (p.Val339=)	rs201434694
NM_022336.4(EDAR):c.146C>T (p.Pro49Leu)	rs375891208
NM_022336.4(EDAR):c.822C>A (p.Ser274=)	rs79648056
NM_022336.4(EDAR):c.844C>T (p.Arg282Trp)	rs781652310

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