ClinVar Miner

List of variants reported as likely pathogenic for Abnormality of esophagus morphology

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 8
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HGVS dbSNP
GRCh37/hg19 11p15.4(chr11:4371631-5253127)
GRCh37/hg19 15q13.3(chr15:32457092-32771537)
GRCh37/hg19 16p13.11-12.3(chr16:14985615-17000304)
GRCh37/hg19 22q11.21(chr22:18637139-20289862)
GRCh37/hg19 2q13(chr2:111186302-113273657)
GRCh37/hg19 4q28.1(chr4:125251081-128286629)
GRCh37/hg19 4q35.2(chr4:187540292-187849681)
GRCh37/hg19 6p22.3(chr6:20884837-21082258)

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