ClinVar Miner

List of variants reported as not provided for Tobacco use disorder by Psychiatry Genetics Yale University

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Total variants: 43
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HGVS dbSNP gnomAD frequency
NM_000744.7(CHRNA4):c.1662G>A (p.Pro554=) rs121912284 0.00165
NM_000744.7(CHRNA4):c.1460G>A (p.Arg487Gln) rs121912280 0.00152
NM_000744.7(CHRNA4):c.462G>A (p.Pro154=) rs121912245 0.00030
NM_000744.7(CHRNA4):c.1711G>A (p.Val571Ile) rs121912285 0.00029
NM_000744.7(CHRNA4):c.1169G>A (p.Gly390Glu) rs121912268 0.00024
NM_000744.7(CHRNA4):c.1635G>A (p.Thr545=) rs121912283 0.00021
NM_000744.7(CHRNA4):c.1373C>T (p.Pro458Leu) rs121912277 0.00013
NM_000744.7(CHRNA4):c.693G>A (p.Pro231=) rs121912250 0.00011
NM_000744.7(CHRNA4):c.948C>T (p.Phe316=) rs121912259 0.00011
NM_000744.7(CHRNA4):c.1228G>A (p.Val410Ile) rs121912272 0.00010
NM_000744.7(CHRNA4):c.1359C>T (p.His453=) rs121912276 0.00009
NM_000744.7(CHRNA4):c.729G>A (p.Pro243=) rs121912253 0.00009
NM_000744.7(CHRNA4):c.963C>T (p.Ile321=) rs121912261 0.00009
NM_000744.7(CHRNA4):c.1087G>A (p.Val363Met) rs121912266 0.00008
NM_000744.7(CHRNA4):c.1266C>T (p.Cys422=) rs121912274 0.00006
NM_000744.7(CHRNA4):c.461C>T (p.Pro154Leu) rs121912244 0.00006
NM_000744.7(CHRNA4):c.1402G>A (p.Val468Ile) rs121912278 0.00004
NM_000744.7(CHRNA4):c.1625C>T (p.Pro542Leu) rs121912281 0.00004
NM_000744.7(CHRNA4):c.585C>G (p.His195Gln) rs121912248 0.00004
NM_000744.7(CHRNA4):c.858C>T (p.Thr286=) rs121912257 0.00004
NM_000744.7(CHRNA4):c.1224C>T (p.Phe408=) rs121912271 0.00003
NM_000744.7(CHRNA4):c.1425C>T (p.Gly475=) rs121912279 0.00003
NM_000744.7(CHRNA4):c.442C>T (p.Arg148Trp) rs121912243 0.00003
NM_000744.7(CHRNA4):c.1054G>A (p.Val352Met) rs121912264 0.00002
NM_000744.7(CHRNA4):c.1109G>A (p.Arg370Gln) rs121912267 0.00002
NM_000744.7(CHRNA4):c.510C>T (p.Phe170=) rs121912247 0.00002
NM_000744.7(CHRNA4):c.1001C>T (p.Ser334Leu) rs121912262 0.00001
NM_000744.7(CHRNA4):c.1184C>T (p.Thr395Met) rs121912269 0.00001
NM_000744.7(CHRNA4):c.1265G>A (p.Cys422Tyr) rs121912273 0.00001
NM_000744.7(CHRNA4):c.1634C>T (p.Thr545Met) rs121912282 0.00001
NM_000744.7(CHRNA4):c.504C>T (p.Phe168=) rs121912246 0.00001
NM_000744.7(CHRNA4):c.617G>C (p.Ser206Thr) rs121912249 0.00001
NM_000744.7(CHRNA4):c.915C>T (p.Leu305=) rs121912258 0.00001
NM_000744.7(CHRNA4):c.1002G>A (p.Ser334=) rs121912263
NM_000744.7(CHRNA4):c.1066C>T (p.Leu356Phe) rs121912265
NM_000744.7(CHRNA4):c.1200C>T (p.Ser400=) rs121912270
NM_000744.7(CHRNA4):c.1311T>C (p.Ala437=) rs121912275
NM_000744.7(CHRNA4):c.705T>C (p.Tyr235=) rs121912251
NM_000744.7(CHRNA4):c.707C>T (p.Ala236Val) rs121912252
NM_000744.7(CHRNA4):c.753C>T (p.Ile251=) rs121912254
NM_000744.7(CHRNA4):c.775T>C (p.Cys259Arg) rs121912255
NM_000744.7(CHRNA4):c.799C>T (p.Leu267=) rs121912256
NM_000744.7(CHRNA4):c.953C>T (p.Thr318Ile) rs121912260

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