ClinVar Miner

List of variants in gene combination DISC1, TSNAX-DISC1 reported as not provided by Psychiatry Genetics Yale University

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Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_018662.3(DISC1):c.791G>A (p.Arg264Gln) rs3738401 0.25560
NM_018662.3(DISC1):c.2063G>A (p.Gly688Glu) rs367543094 0.00041
NM_018662.3(DISC1):c.1518A>G (p.Pro506=) rs367543091 0.00029
NM_018662.3(DISC1):c.2550C>T (p.His850=) rs367543100 0.00022
NM_018662.3(DISC1):c.2295T>A (p.Gly765=) rs367543098 0.00013
NM_018662.3(DISC1):c.1729A>G (p.Lys577Glu) rs367543093 0.00006
NM_018662.3(DISC1):c.768C>T (p.His256=) rs367543085 0.00006
NM_018662.3(DISC1):c.1718C>T (p.Thr573Ile) rs367543092 0.00003
NM_018662.3(DISC1):c.2543G>A (p.Gly848Asp) rs367543099 0.00003
NM_018662.3(DISC1):c.2157G>A (p.Glu719=) rs367543095 0.00002
NM_018662.3(DISC1):c.1363C>T (p.Arg455Ter) rs367543089 0.00001
NM_018662.3(DISC1):c.2215G>A (p.Glu739Lys) rs367543096 0.00001
NM_018662.3(DISC1):c.2221A>G (p.Lys741Glu) rs367543097 0.00001
NM_018662.3(DISC1):c.841G>A (p.Ala281Thr) rs367543086 0.00001
NM_018662.3(DISC1):c.1286C>G (p.Thr429Ser) rs367543087
NM_018662.3(DISC1):c.1291A>G (p.Thr431Ala) rs367543088
NM_018662.3(DISC1):c.1401A>G (p.Lys467=) rs367543090
NM_018662.3(DISC1):c.340A>T (p.Thr114Ser) rs367543083
NM_018662.3(DISC1):c.472G>A (p.Ala158Thr) rs367543084

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