ClinVar Miner

List of variants in gene DBH reported as uncertain significance by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 89
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HGVS dbSNP gnomAD frequency
NM_000787.4(DBH):c.*393C>T rs565769234 0.00634
NM_000787.4(DBH):c.*415C>T rs533447101 0.00285
NM_000787.4(DBH):c.1444G>A (p.Gly482Arg) rs41316996 0.00180
NM_000787.4(DBH):c.490G>A (p.Gly164Ser) rs142383279 0.00077
NM_000787.4(DBH):c.*319C>T rs866646852 0.00069
NM_000787.4(DBH):c.1215C>T (p.His405=) rs144219953 0.00068
NM_000787.4(DBH):c.165G>A (p.Pro55=) rs139591190 0.00057
NM_000787.4(DBH):c.1788C>T (p.Cys596=) rs61729385 0.00051
NM_000787.4(DBH):c.632C>T (p.Ala211Val) rs143535251 0.00051
NM_000787.4(DBH):c.807C>T (p.Cys269=) rs141816448 0.00050
NM_000787.4(DBH):c.1516G>A (p.Ala506Thr) rs148439785 0.00048
NM_000787.4(DBH):c.892G>A (p.Val298Met) rs145655199 0.00044
NM_000787.4(DBH):c.583G>A (p.Val195Met) rs145059403 0.00040
NM_000787.4(DBH):c.849C>T (p.Cys283=) rs78200745 0.00040
NM_000787.4(DBH):c.253G>A (p.Val85Ile) rs78445536 0.00038
NM_000787.4(DBH):c.1025-6T>A rs199926239 0.00034
NM_000787.4(DBH):c.1643A>G (p.Asn548Ser) rs151228388 0.00029
NM_000787.4(DBH):c.1028G>A (p.Arg343Gln) rs369664655 0.00028
NM_000787.4(DBH):c.*320G>A rs561965972 0.00027
NM_000787.4(DBH):c.291C>T (p.Asn97=) rs75734048 0.00022
NM_000787.4(DBH):c.717G>C (p.Lys239Asn) rs5321 0.00021
NM_000787.4(DBH):c.*431C>T rs551208345 0.00020
NM_000787.4(DBH):c.1688T>C (p.Met563Thr) rs201973877 0.00019
NM_000787.4(DBH):c.1840G>A (p.Gly614Arg) rs76316834 0.00017
NM_000787.4(DBH):c.354C>T (p.Asp118=) rs199898782 0.00017
NM_000787.4(DBH):c.*845G>A rs769087490 0.00016
NM_000787.4(DBH):c.1139G>A (p.Arg380Gln) rs77984399 0.00016
NM_000787.4(DBH):c.1198C>T (p.Pro400Ser) rs200798319 0.00012
NM_000787.4(DBH):c.*318C>A rs140355168 0.00011
NM_000787.4(DBH):c.*52G>A rs531831034 0.00011
NM_000787.4(DBH):c.1493C>T (p.Thr498Met) rs78512658 0.00011
NM_000787.4(DBH):c.*401C>T rs886063665 0.00010
NM_000787.4(DBH):c.1094T>C (p.Met365Thr) rs200103371 0.00010
NM_000787.4(DBH):c.1451T>C (p.Leu484Pro) rs769107895 0.00010
NM_000787.4(DBH):c.*414C>G rs960670938 0.00008
NM_000787.4(DBH):c.1599G>A (p.Ala533=) rs377563744 0.00008
NM_000787.4(DBH):c.624C>T (p.Pro208=) rs75942058 0.00008
NM_000787.4(DBH):c.1173G>A (p.Thr391=) rs201689325 0.00007
NM_000787.4(DBH):c.*283A>C rs886063661 0.00006
NM_000787.4(DBH):c.*73C>T rs1012869106 0.00006
NM_000787.4(DBH):c.1001A>T (p.Tyr334Phe) rs200678652 0.00006
NM_000787.4(DBH):c.1835T>C (p.Ile612Thr) rs372197370 0.00006
NM_000787.4(DBH):c.1722+13G>T rs200197329 0.00005
NM_000787.4(DBH):c.1148C>T (p.Ala383Val) rs756212220 0.00004
NM_000787.4(DBH):c.1286G>A (p.Arg429Gln) rs773007874 0.00004
NM_000787.4(DBH):c.1365G>A (p.Ser455=) rs369001369 0.00004
NM_000787.4(DBH):c.*213A>C rs578112069 0.00003
NM_000787.4(DBH):c.*222C>T rs561913284 0.00003
NM_000787.4(DBH):c.*425C>T rs895219061 0.00003
NM_000787.4(DBH):c.486+15C>T rs749887039 0.00003
NM_000787.4(DBH):c.776C>T (p.Ala259Val) rs201600007 0.00003
NM_000787.4(DBH):c.983T>G (p.Leu328Arg) rs764045527 0.00003
NM_000787.4(DBH):c.*649C>T rs777802512 0.00002
NM_000787.4(DBH):c.*698C>T rs896192061 0.00002
NM_000787.4(DBH):c.1563-3C>T rs540054463 0.00002
NM_000787.4(DBH):c.*315G>A rs886063662 0.00001
NM_000787.4(DBH):c.*383C>T rs886063663 0.00001
NM_000787.4(DBH):c.*482C>T rs1040634911 0.00001
NM_000787.4(DBH):c.*846G>A rs886063668 0.00001
NM_000787.4(DBH):c.1155C>T (p.Ile385=) rs752651309 0.00001
NM_000787.4(DBH):c.128G>A (p.Arg43His) rs779109570 0.00001
NM_000787.4(DBH):c.1300G>A (p.Val434Met) rs372010353 0.00001
NM_000787.4(DBH):c.1825G>A (p.Val609Ile) rs141570582 0.00001
NM_000787.4(DBH):c.259T>C (p.Phe87Leu) rs761327487 0.00001
NM_000787.4(DBH):c.407T>C (p.Val136Ala) rs886063657 0.00001
NM_000787.4(DBH):c.921+8C>T rs886063659 0.00001
NM_000787.4(DBH):c.*116G>A rs886063660
NM_000787.4(DBH):c.*180A>G rs1832368444
NM_000787.4(DBH):c.*253C>G rs749898125
NM_000787.4(DBH):c.*268A>G rs1832369760
NM_000787.4(DBH):c.*389_*390insACCCCC rs1554737844
NM_000787.4(DBH):c.*398C>T rs1832372715
NM_000787.4(DBH):c.*459A>G rs886063666
NM_000787.4(DBH):c.*493C>T rs1044246377
NM_000787.4(DBH):c.*565_*566del rs775021806
NM_000787.4(DBH):c.1128C>A (p.Ala376=) rs763415382
NM_000787.4(DBH):c.1434+9C>T rs1832270556
NM_000787.4(DBH):c.153C>G (p.Ile51Met) rs1832054587
NM_000787.4(DBH):c.1556T>C (p.Ile519Thr) rs537856898
NM_000787.4(DBH):c.1557C>T (p.Ile519=) rs764026303
NM_000787.4(DBH):c.16C>A (p.Arg6Ser) rs111514228
NM_000787.4(DBH):c.1813G>A (p.Ala605Thr) rs1832363886
NM_000787.4(DBH):c.363G>A (p.Gly121=) rs763997950
NM_000787.4(DBH):c.450C>T (p.Pro150=) rs150007277
NM_000787.4(DBH):c.61A>G (p.Met21Val) rs1381096496
NM_000787.4(DBH):c.686C>A (p.Thr229Lys) rs200628504
NM_000787.4(DBH):c.736A>G (p.Ile246Val) rs983397516
NM_000787.4(DBH):c.852C>T (p.Asp284=) rs886063658
NM_000787.4(DBH):c.932A>G (p.Tyr311Cys) rs560578268

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