ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 14
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HGVS dbSNP gnomAD frequency
NM_006371.5(CRTAP):c.*2474T>G rs78745278 0.01414
NM_006371.5(CRTAP):c.*3950G>A rs141093723 0.00541
NM_006371.5(CRTAP):c.*2876C>T rs147135876 0.00540
NM_006371.5(CRTAP):c.*4017G>A rs115504052 0.00534
NM_006371.5(CRTAP):c.*4129T>C rs76450273 0.00503
NM_006371.5(CRTAP):c.*4705G>T rs145711257 0.00483
NM_006371.5(CRTAP):c.*2943A>G rs115684525 0.00447
NM_006371.5(CRTAP):c.*3454C>T rs140429132 0.00417
NM_006371.5(CRTAP):c.*288C>T rs111603077 0.00336
NM_006371.5(CRTAP):c.*1041C>T rs114487086 0.00282
NM_006371.5(CRTAP):c.*31C>T rs149138748 0.00240
NM_006371.5(CRTAP):c.*2524G>A rs150800828 0.00234
NM_006371.5(CRTAP):c.*1124C>A rs570473174 0.00096
NM_006371.5(CRTAP):c.*1861A>G rs553553619 0.00007

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