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#609621 - SHORT QT SYNDROME 2; SQT2
Cytogenetic locations: Heterotaxy
Gene summaries Genetic tests Medical literature
#607554 - ATRIAL FIBRILLATION, FAMILIAL, 3; ATFB3
*607542 - POTASSIUM CHANNEL, VOLTAGE-GATED, KQT-LIKE SUBFAMILY, MEMBER 1; KCNQ1
#220400 - JERVELL AND LANGE-NIELSEN SYNDROME 1; JLNS1
#192500 - LONG QT SYNDROME 1; LQT1
LONG QT SYNDROME 1/2, DIGENIC, INCLUDED; LQT1/2, DIGENIC, INCLUDED
#130650 - BECKWITH-WIEDEMANN SYNDROME; BWS
BECKWITH-WIEDEMANN SYNDROME CHROMOSOME REGION, INCLUDED; BWCR, INCLUDED
Cytogenetic locations: 1p36, 1p36, 606238
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