List of variants in gene ANK2 reported as uncertain significance by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 32

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HGVS	dbSNP	gnomAD frequency
NM_001148.6(ANK2):c.3796+18G>A	rs66792339	0.02360
NM_001148.6(ANK2):c.11009C>A (p.Thr3670Asn)	rs45608232	0.00029
NM_001148.6(ANK2):c.11032+19A>G	rs200769962	0.00016
NM_001148.6(ANK2):c.11354A>G (p.Gln3785Arg)	rs150808807	0.00006
NM_001148.6(ANK2):c.3572G>A (p.Arg1191Gln)	rs780110299	0.00003
NM_001148.6(ANK2):c.4912A>G (p.Asn1638Asp)	rs748573794	0.00003
NM_001148.6(ANK2):c.8417T>C (p.Val2806Ala)	rs769091762	0.00003
NM_001148.6(ANK2):c.10646G>A (p.Arg3549His)	rs768351547	0.00002
NM_001148.6(ANK2):c.2044C>G (p.Leu682Val)	rs749503484	0.00002
NM_001148.6(ANK2):c.3067G>A (p.Gly1023Arg)	rs151127289	0.00002
NM_001148.6(ANK2):c.9703C>T (p.Pro3235Ser)	rs202098889	0.00002
NM_001148.6(ANK2):c.10562C>T (p.Pro3521Leu)	rs766421377	0.00001
NM_001148.6(ANK2):c.10645C>T (p.Arg3549Cys)	rs1056477885	0.00001
NM_001148.6(ANK2):c.1783-4A>G	rs755543636	0.00001
NM_001148.6(ANK2):c.4045A>G (p.Met1349Val)	rs765236990	0.00001
NM_001148.6(ANK2):c.4393C>A (p.Gln1465Lys)	rs761254386	0.00001
NM_001148.6(ANK2):c.6601A>G (p.Ser2201Gly)	rs201717651	0.00001
NM_001148.6(ANK2):c.9145C>T (p.Arg3049Trp)	rs1201870166	0.00001
NM_001148.6(ANK2):c.10054G>C (p.Val3352Leu)
NM_001148.6(ANK2):c.10310T>C (p.Ile3437Thr)	rs886039169
NM_001148.6(ANK2):c.10425A>G (p.Ile3475Met)	rs1554572397
NM_001148.6(ANK2):c.11032+17G>A	rs587780853
NM_001148.6(ANK2):c.11540T>A (p.Val3847Glu)	rs1554590569
NM_001148.6(ANK2):c.11807A>G (p.Tyr3936Cys)	rs377555678
NM_001148.6(ANK2):c.2396C>T (p.Ala799Val)	rs776957456
NM_001148.6(ANK2):c.2460CAC[6] (p.Thr826dup)	rs770530257
NM_001148.6(ANK2):c.266C>A (p.Ser89Tyr)
NM_001148.6(ANK2):c.2900+5G>A	rs768275410
NM_001148.6(ANK2):c.4055A>G (p.Asp1352Gly)	rs2153979257
NM_001148.6(ANK2):c.4371+19T>C	rs1057522286
NM_001148.6(ANK2):c.8133G>T (p.Gln2711His)	rs771607762
NM_001148.6(ANK2):c.9751G>C (p.Ala3251Pro)	rs2095950515

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