List of variants in gene ANK2 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: 28

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HGVS	dbSNP	gnomAD frequency
NM_001148.6(ANK2):c.8503C>T (p.Pro2835Ser)	rs3733617	0.14405
NM_001148.6(ANK2):c.3510A>G (p.Val1170=)	rs35336373	0.02906
NM_001148.6(ANK2):c.3796+18G>A	rs66792339	0.02360
NM_001148.6(ANK2):c.9900C>A (p.Ser3300Arg)	rs34270799	0.01986
NM_001148.6(ANK2):c.6634G>A (p.Gly2212Ser)	rs61734478	0.01567
NM_001148.6(ANK2):c.3893+10T>C	rs72556367	0.01042
NM_001148.6(ANK2):c.11218C>A (p.Leu3740Ile)	rs35530544	0.01031
NM_001148.6(ANK2):c.11790C>T (p.Ile3930=)	rs45517840	0.00954
NM_001148.6(ANK2):c.9854T>C (p.Ile3285Thr)	rs36210417	0.00822
NM_001148.6(ANK2):c.3379+12T>G	rs139528815	0.00812
NM_001148.6(ANK2):c.9996T>C (p.Ser3332=)	rs145557320	0.00778
NM_001148.6(ANK2):c.2377-8C>T	rs139893914	0.00682
NM_001148.6(ANK2):c.2178+18C>T	rs45447896	0.00674
NM_001148.6(ANK2):c.1881+8C>G	rs74976371	0.00612
NM_001148.6(ANK2):c.2278-11G>A	rs146312675	0.00538
NM_001148.6(ANK2):c.9454A>G (p.Thr3152Ala)	rs61741040	0.00340
NM_001148.6(ANK2):c.10395G>A (p.Glu3465=)	rs147423696	0.00282
NM_001148.6(ANK2):c.4152T>C (p.Asp1384=)	rs116128106	0.00267
NM_001148.6(ANK2):c.3543C>T (p.Ala1181=)	rs76685232	0.00265
NM_001148.6(ANK2):c.3366C>T (p.Asn1122=)	rs114896457	0.00256
NM_001148.6(ANK2):c.9286A>G (p.Ser3096Gly)	rs144158934	0.00238
NM_001148.6(ANK2):c.6648C>G (p.Gly2216=)	rs140926982	0.00208
NM_001148.6(ANK2):c.11860-18T>G	rs138978479	0.00207
NM_001148.6(ANK2):c.6633C>T (p.Ala2211=)	rs143516811	0.00018
NM_001148.6(ANK2):c.2249A>G (p.Gln750Arg)	rs371787039	0.00014
NM_001148.6(ANK2):c.813T>C (p.His271=)	rs774848857	0.00005
NM_001148.6(ANK2):c.11032+20TG[13]	rs34201791
NM_001148.6(ANK2):c.11032+20TG[17]	rs34201791

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