List of variants reported as risk factor by Neurogenetics Research Program, University of Adelaide

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_000506.5(F2):c.*97G>A	rs1799963	0.00979
NM_000506.3(F2):c.598G>A (p.Glu200Lys)	rs62623459	0.00138
GRCh37/hg19 15q11.2-12(chr15:22722801-26749200)
GRCh37/hg19 1q21.1(chr1:145382601-145616000)
GRCh37/hg19 9q33.1(chr9:119311659-119462832)
NM_000132.4(F8):c.5146C>A (p.His1716Asn)	rs2073172888
NM_001136271.3(NKX2-6):c.455dup (p.Gln153fs)	rs757292066

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