ClinVar Miner

List of variants in gene SCN1B studied for Cardiac conduction defect, nonspecific

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Total variants: 15
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NM_001037.5(SCN1B):c.-132C>G rs886054339
NM_001037.5(SCN1B):c.-27G>C rs758958222
NM_001037.5(SCN1B):c.-88A>C rs886054341
NM_001037.5(SCN1B):c.-93G>C rs886054340
NM_001037.5(SCN1B):c.-95C>T rs569134158
NM_001037.5(SCN1B):c.-9C>A rs66671189
NM_001037.5(SCN1B):c.150C>T (p.Asn50=) rs147073518
NM_001037.5(SCN1B):c.207+14G>A rs16969924
NM_001037.5(SCN1B):c.259G>C (p.Glu87Gln) rs121434627
NM_001037.5(SCN1B):c.28G>A (p.Gly10Ser) rs72552027
NM_001037.5(SCN1B):c.351C>T (p.Gly117=) rs3746255
NM_001037.5(SCN1B):c.40+15G>T rs72556351
NM_001037.5(SCN1B):c.412G>A (p.Val138Ile) rs72558029
NM_001037.5(SCN1B):c.448+89G>A rs267607029
NM_001037.5(SCN1B):c.501T>C (p.Ile167=) rs16969930

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