List of variants in gene ANK3 reported as uncertain significance by New York Genome Center

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_020987.5(ANK3):c.11678G>C (p.Ser3893Thr)	rs12260663	0.00044
NM_020987.5(ANK3):c.6555G>T (p.Gln2185His)	rs144465058	0.00036
NM_020987.5(ANK3):c.3488A>G (p.Gln1163Arg)	rs746416574	0.00009
NM_020987.5(ANK3):c.3970G>A (p.Val1324Ile)	rs755265993	0.00006
NM_020987.5(ANK3):c.5183C>T (p.Ser1728Phe)	rs759998919	0.00006
NM_001204403.2(ANK3):c.13G>T (p.Ala5Ser)	rs777570818	0.00004
NM_020987.5(ANK3):c.1657G>A (p.Asp553Asn)	rs753197813	0.00003
NM_020987.5(ANK3):c.9252G>T (p.Glu3084Asp)	rs759850374	0.00002
NM_020987.5(ANK3):c.12229A>C (p.Ser4077Arg)	rs778664446	0.00001
NM_020987.5(ANK3):c.1491+4T>C	rs765680287	0.00001
NM_020987.5(ANK3):c.1939G>A (p.Ala647Thr)	rs761904426	0.00001
NM_020987.5(ANK3):c.4705T>G (p.Ser1569Ala)	rs375050420	0.00001
NM_020987.5(ANK3):c.11591A>G (p.Lys3864Arg)
NM_020987.5(ANK3):c.2836G>C (p.Glu946Gln)	rs2094230190
NM_020987.5(ANK3):c.9598A>G (p.Ile3200Val)	rs2131970999

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