ClinVar Miner

List of variants in gene SPRED1 reported as likely benign by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_152594.3(SPRED1):c.*2885G>A rs79309779 0.01111
NM_152594.3(SPRED1):c.*3057A>G rs72725362 0.01073
NM_152594.3(SPRED1):c.*3591C>T rs147489619 0.00493
NM_152594.3(SPRED1):c.*1040G>A rs115568221 0.00420
NM_152594.3(SPRED1):c.*2570T>C rs111997668 0.00408
NM_152594.3(SPRED1):c.*3623G>T rs148525432 0.00324
NM_152594.3(SPRED1):c.*3561G>A rs181980647 0.00234
NM_152594.3(SPRED1):c.*4372A>G rs187788660 0.00113
NM_152594.3(SPRED1):c.675C>T (p.Ser225=) rs144764225 0.00092
NM_152594.3(SPRED1):c.-191C>T rs556907443 0.00089
NM_152594.3(SPRED1):c.702C>G (p.Ile234Met) rs138553244 0.00074
NM_152594.3(SPRED1):c.939G>A (p.Thr313=) rs140644874 0.00070
NM_152594.3(SPRED1):c.*4697G>A rs188784206 0.00048
NM_152594.3(SPRED1):c.30C>A (p.Asn10Lys) rs201692618 0.00042
NM_152594.3(SPRED1):c.*633A>G rs118146919 0.00037
NM_152594.3(SPRED1):c.*2247A>G rs118057877 0.00022
NM_152594.3(SPRED1):c.*2018T>G rs188392935 0.00016
NM_152594.3(SPRED1):c.*5202C>T rs541213700 0.00001
NM_152594.3(SPRED1):c.*1659_*1662del rs57589132
NM_152594.3(SPRED1):c.*2611C>T rs181716461
NM_152594.3(SPRED1):c.*5090dup rs141174183
NM_152594.3(SPRED1):c.*581T>C rs541503324

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