ClinVar Miner

List of variants in gene combination GOSR2, LRRC37A2 reported as uncertain significance for brain disorder

Included ClinVar conditions (1840):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 109
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HGVS dbSNP gnomAD frequency
NM_004287.5(GOSR2):c.*1377G>A rs180777362 0.00573
NM_004287.5(GOSR2):c.*1679A>G rs149765350 0.00273
NM_004287.5(GOSR2):c.40G>A (p.Glu14Lys) rs113817924 0.00232
NM_004287.5(GOSR2):c.*2057C>T rs368549324 0.00180
NM_004287.5(GOSR2):c.*2336A>T rs569751775 0.00055
NM_004287.5(GOSR2):c.*1703A>G rs144662292 0.00053
NM_004287.5(GOSR2):c.*2192T>G rs545130658 0.00034
NM_004287.5(GOSR2):c.509A>G (p.Asn170Ser) rs150907052 0.00031
NM_004287.5(GOSR2):c.29+8C>T rs573306680 0.00029
NM_004287.5(GOSR2):c.*2291C>G rs186093347 0.00021
NM_004287.5(GOSR2):c.*1446A>T rs572361575 0.00016
NM_004287.5(GOSR2):c.94+7A>C rs376231923 0.00016
NM_004287.5(GOSR2):c.336+9G>A rs200210055 0.00013
NM_004287.5(GOSR2):c.552G>T (p.Lys184Asn) rs760846460 0.00012
NM_004287.5(GOSR2):c.393G>T (p.Gln131His) rs182039780 0.00006
NM_004287.5(GOSR2):c.547G>A (p.Glu183Lys) rs144472114 0.00005
NM_004287.5(GOSR2):c.404A>G (p.Asn135Ser) rs765513191 0.00004
NM_004287.5(GOSR2):c.637T>C (p.Ter213Arg) rs1229223114 0.00004
NM_004287.5(GOSR2):c.80A>G (p.Lys27Arg) rs373000501 0.00004
NM_004287.5(GOSR2):c.*18G>T rs778066395 0.00003
NM_004287.5(GOSR2):c.*2253C>T rs886053085 0.00003
NM_004287.5(GOSR2):c.29+13C>T rs747791818 0.00003
NM_004287.5(GOSR2):c.340T>C (p.Ser114Pro) rs751635119 0.00003
NM_004287.5(GOSR2):c.510C>G (p.Asn170Lys) rs34572603 0.00003
NM_004287.5(GOSR2):c.538C>T (p.Arg180Trp) rs1305687118 0.00003
NM_004287.5(GOSR2):c.57G>A (p.Met19Ile) rs369247929 0.00003
NM_004287.5(GOSR2):c.619G>A (p.Val207Met) rs780839289 0.00003
NM_004287.5(GOSR2):c.71C>T (p.Thr24Met) rs528931142 0.00003
NM_004287.5(GOSR2):c.8C>A (p.Pro3His) rs1131691533 0.00003
NM_004287.5(GOSR2):c.*1277C>G rs577505377 0.00002
NM_004287.5(GOSR2):c.*2195C>A rs565638240 0.00002
NM_004287.5(GOSR2):c.563A>G (p.Gln188Arg) rs776748629 0.00002
NM_004287.5(GOSR2):c.579G>A (p.Met193Ile) rs768377570 0.00002
NM_004287.5(GOSR2):c.68A>G (p.Glu23Gly) rs200071814 0.00002
NM_004287.5(GOSR2):c.94+5G>A rs754004382 0.00002
NM_004287.5(GOSR2):c.*2213G>T rs886053084 0.00001
NM_004287.5(GOSR2):c.*2589T>C rs886053087 0.00001
NM_004287.5(GOSR2):c.10C>G (p.Leu4Val) rs756276963 0.00001
NM_004287.5(GOSR2):c.14T>A (p.Phe5Tyr) rs897281647 0.00001
NM_004287.5(GOSR2):c.1A>G (p.Met1Val) rs879328855 0.00001
NM_004287.5(GOSR2):c.28A>G (p.Lys10Glu) rs1278419518 0.00001
NM_004287.5(GOSR2):c.29+3G>A rs794726915 0.00001
NM_004287.5(GOSR2):c.331A>G (p.Thr111Ala) rs780448159 0.00001
NM_004287.5(GOSR2):c.336C>T (p.Asn112=) rs755211944 0.00001
NM_004287.5(GOSR2):c.358A>G (p.Met120Val) rs769454681 0.00001
NM_004287.5(GOSR2):c.364G>A (p.Glu122Lys) rs374613085 0.00001
NM_004287.5(GOSR2):c.371T>C (p.Leu124Pro) rs1189596801 0.00001
NM_004287.5(GOSR2):c.451C>G (p.Leu151Val) rs756144831 0.00001
NM_004287.5(GOSR2):c.541C>G (p.Leu181Val) rs772342696 0.00001
NM_004287.5(GOSR2):c.553C>T (p.Arg185Trp) rs771037415 0.00001
NM_004287.5(GOSR2):c.55A>G (p.Met19Val) rs770329469 0.00001
NM_004287.5(GOSR2):c.56T>C (p.Met19Thr) rs374861039 0.00001
NM_004287.5(GOSR2):c.77A>G (p.Asp26Gly) rs773543394 0.00001
NM_004287.5(GOSR2):c.94+4A>G rs796052540 0.00001
NM_004287.4(GOSR2):c.-64G>T rs886053076
NM_004287.5(GOSR2):c.*1105A>T rs780111337
NM_004287.5(GOSR2):c.*2068C>G rs886053082
NM_004287.5(GOSR2):c.*2190TC[2] rs553512648
NM_004287.5(GOSR2):c.*2573G>A rs886053086
NM_004287.5(GOSR2):c.*286G>T rs78693564
NM_004287.5(GOSR2):c.*332A>G rs886053079
NM_004287.5(GOSR2):c.*412C>A rs886053080
NM_004287.5(GOSR2):c.*804A>G rs886053081
NM_004287.5(GOSR2):c.-20T>G rs886053077
NM_004287.5(GOSR2):c.-7C>G rs760018200
NM_004287.5(GOSR2):c.15C>G (p.Phe5Leu) rs2085950798
NM_004287.5(GOSR2):c.20A>G (p.Gln7Arg) rs2085951116
NM_004287.5(GOSR2):c.29+13C>A
NM_004287.5(GOSR2):c.31C>G (p.Gln11Glu) rs2146850344
NM_004287.5(GOSR2):c.320G>C (p.Arg107Pro) rs750960207
NM_004287.5(GOSR2):c.350C>T (p.Thr117Ile) rs1599019391
NM_004287.5(GOSR2):c.354A>G (p.Ile118Met)
NM_004287.5(GOSR2):c.363C>T (p.Asp121=) rs886053078
NM_004287.5(GOSR2):c.374A>G (p.Gln125Arg)
NM_004287.5(GOSR2):c.380A>G (p.Asn127Ser)
NM_004287.5(GOSR2):c.383C>A (p.Ser128Tyr)
NM_004287.5(GOSR2):c.397G>A (p.Val133Ile)
NM_004287.5(GOSR2):c.3G>A (p.Met1Ile) rs1174104260
NM_004287.5(GOSR2):c.3G>T (p.Met1Ile)
NM_004287.5(GOSR2):c.406G>A (p.Gly136Ser)
NM_004287.5(GOSR2):c.428A>T (p.Asp143Val) rs2088079257
NM_004287.5(GOSR2):c.432_449del (p.His145_Gly150del) rs1381386644
NM_004287.5(GOSR2):c.439A>G (p.Ile147Val) rs757363374
NM_004287.5(GOSR2):c.446A>G (p.Asp149Gly) rs2088083666
NM_004287.5(GOSR2):c.460_461dup (p.Gln154fs)
NM_004287.5(GOSR2):c.477+6G>T rs1568177911
NM_004287.5(GOSR2):c.478-7_478-6insAGAACAGAAG
NM_004287.5(GOSR2):c.478G>C (p.Gly160Arg)
NM_004287.5(GOSR2):c.47A>C (p.Gln16Pro) rs746688685
NM_004287.5(GOSR2):c.494T>C (p.Ile165Thr)
NM_004287.5(GOSR2):c.4G>A (p.Asp2Asn) rs1425442098
NM_004287.5(GOSR2):c.506C>G (p.Ala169Gly) rs2088814830
NM_004287.5(GOSR2):c.50C>T (p.Ser17Phe)
NM_004287.5(GOSR2):c.524C>A (p.Ser175Tyr)
NM_004287.5(GOSR2):c.539G>A (p.Arg180Gln) rs1348639194
NM_004287.5(GOSR2):c.557_584del (p.Ala186fs) rs796052541
NM_004287.5(GOSR2):c.568A>G (p.Lys190Glu) rs765094724
NM_004287.5(GOSR2):c.578T>C (p.Met193Thr) rs1328118330
NM_004287.5(GOSR2):c.596T>C (p.Leu199Pro)
NM_004287.5(GOSR2):c.611T>G (p.Met204Arg) rs2147051685
NM_004287.5(GOSR2):c.619G>T (p.Val207Leu) rs780839289
NM_004287.5(GOSR2):c.634A>G (p.Thr212Ala) rs956070241
NM_004287.5(GOSR2):c.639A>G (p.Ter213Trp) rs2147052419
NM_004287.5(GOSR2):c.6T>A (p.Asp2Glu)
NM_004287.5(GOSR2):c.79A>C (p.Lys27Gln) rs760997502
NM_004287.5(GOSR2):c.7C>G (p.Pro3Ala) rs12944167
NM_004287.5(GOSR2):c.7C>T (p.Pro3Ser) rs12944167
NM_004287.5(GOSR2):c.92A>G (p.His31Arg)
NM_004287.5(GOSR2):c.94A>G (p.Ile32Val) rs2086996915

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