ClinVar Miner

List of variants in gene combination FZD4, PRSS23 reported as benign for central nervous system disorder

Included ClinVar conditions (2498):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 45
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HGVS dbSNP gnomAD frequency
NM_012193.4(FZD4):c.*1298C>T rs3802892 0.70569
NM_012193.4(FZD4):c.*4664T>C rs713065 0.56868
NM_012193.4(FZD4):c.*2971T>C rs10898563 0.27626
NM_012193.4(FZD4):c.*4765T>C rs72963441 0.03760
NM_012193.4(FZD4):c.*5077C>G rs143372848 0.02078
NM_012193.4(FZD4):c.*2G>T rs61749246 0.01897
NM_012193.4(FZD4):c.*3700A>G rs115341334 0.01592
NM_012193.4(FZD4):c.*4196A>G rs138561450 0.01587
NM_012193.4(FZD4):c.*5368C>T rs79807722 0.01583
NM_012193.4(FZD4):c.*3574C>T rs78806773 0.01478
NM_012193.4(FZD4):c.*1932G>C rs77424184 0.01431
NM_012193.4(FZD4):c.502C>T (p.Pro168Ser) rs61735303 0.01408
NM_012193.4(FZD4):c.*203A>G rs3740661 0.01278
NM_012193.4(FZD4):c.*4775C>T rs61903831 0.01158
NM_012193.4(FZD4):c.*2660C>T rs11234890 0.01129
NM_012193.4(FZD4):c.*2581G>T rs60226660 0.00774
NM_012193.4(FZD4):c.*2542T>C rs115557428 0.00769
NM_012193.4(FZD4):c.*5451G>A rs58750277 0.00668
NM_012193.4(FZD4):c.*827A>G rs61088092 0.00664
NM_012193.4(FZD4):c.*3402G>T rs139460265 0.00650
NM_012193.4(FZD4):c.*4335T>C rs141874425 0.00612
NM_012193.4(FZD4):c.*2101C>G rs77034986 0.00599
NM_012193.4(FZD4):c.*764T>C rs145679440 0.00573
NM_012193.4(FZD4):c.*947G>A rs141895567 0.00396
NM_012193.4(FZD4):c.*4883G>T rs147967476 0.00280
NM_012193.4(FZD4):c.*2639A>G rs145929150 0.00265
NM_012193.4(FZD4):c.*3639A>G rs577322047 0.00073
NM_012193.4(FZD4):c.*3775C>T rs112177728 0.00051
NM_012193.4(FZD4):c.*3770A>T rs182049165 0.00040
NM_012193.4(FZD4):c.*1481C>T rs149837228 0.00021
NM_012193.4(FZD4):c.*4518C>G rs542033644 0.00019
NM_012193.4(FZD4):c.*135C>T rs377696818 0.00016
NM_012193.4(FZD4):c.1405G>A (p.Ala469Thr) rs185157734 0.00016
NM_012193.4(FZD4):c.*4079G>A rs562725038 0.00014
NM_012193.4(FZD4):c.1589G>A (p.Gly530Glu) rs201256460 0.00010
NM_012193.4(FZD4):c.*4618G>A rs147043943 0.00007
NM_012193.4(FZD4):c.*647A>G rs552492300 0.00006
NM_012193.4(FZD4):c.1009C>A (p.His337Asn) rs146895719 0.00006
NM_012193.4(FZD4):c.*799A>G rs573013571 0.00005
NM_012193.4(FZD4):c.*3888G>A rs541479825 0.00004
NM_012193.4(FZD4):c.*128G>A rs530994733 0.00001
NM_012193.4(FZD4):c.*2517A>G rs556412849 0.00001
NM_012193.4(FZD4):c.1440A>G (p.Lys480=) rs751738021 0.00001
NM_012193.4(FZD4):c.*2047C>T rs527339048
NM_012193.4(FZD4):c.*2960T>C rs59987244

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