rs7626962(T) allele has been reported to increase the risk for cardiac issues such as long QT syndrome but also arrhythmias and even sudden infant death syndrome.
rs7626962 is located at position chr3:38595911, Build 116, within the SCN5A gene (Accession No. NT 022517).
The SCN5A gene codes for the sodium channel, voltage-gated, type V, alpha (long QT syndrome 3) protein. This protein produces sodium channels that transport sodium ions across cell membranes and plays a key role in generating and transmitting electrical signals.
Covered by US Patent US8027791B2
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Disease:
Sudden Cardiac Arrest
Accession Type:
dbSNP Id
Accession Number:
rs7626962
Variant Type:
Missense
ACMG:
Compliant
Not compliant
Curated Literature:
Yes
No
Population Data:
Yes
No
Case/Segregation:
Yes
No
Evidence Summary:
Yes
No
List of Resources:
Yes
No
Data Download:
Yes