ClinVar Miner

List of variants reported as benign for Buschke-Ollendorff syndrome by Illumina Clinical Services Laboratory,Illumina

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 23
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HGVS dbSNP
NM_014319.5(LEMD3):c.*1156G>A rs11175698
NM_014319.5(LEMD3):c.*1481C>T rs113095916
NM_014319.5(LEMD3):c.*1635G>A rs12304180
NM_014319.5(LEMD3):c.*1880C>T rs2888
NM_014319.5(LEMD3):c.*1901G>A rs12071
NM_014319.5(LEMD3):c.*1951C>T rs11175699
NM_014319.5(LEMD3):c.*225A>G rs139476203
NM_014319.5(LEMD3):c.*476C>T rs144515474
NM_014319.5(LEMD3):c.*655C>T rs12302249
NM_014319.5(LEMD3):c.*688T>C rs188087693
NM_014319.5(LEMD3):c.*884A>G rs117029005
NM_014319.5(LEMD3):c.*895T>C rs182177872
NM_014319.5(LEMD3):c.*902G>A rs145080926
NM_014319.5(LEMD3):c.*915G>T rs117013092
NM_014319.5(LEMD3):c.1523-12C>T rs11175678
NM_014319.5(LEMD3):c.1560+10C>T rs144815611
NM_014319.5(LEMD3):c.1628-11A>C rs6581620
NM_014319.5(LEMD3):c.1695+8A>G rs6581621
NM_014319.5(LEMD3):c.2305+4T>C rs138310805
NM_014319.5(LEMD3):c.2658G>A (p.Lys886=) rs17101179
NM_014319.5(LEMD3):c.336C>T (p.Ala112=) rs61736594
NM_014319.5(LEMD3):c.378C>T (p.Ser126=) rs61736593
NM_014319.5(LEMD3):c.948C>T (p.Leu316=) rs183253527

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