ClinVar Miner

List of variants in gene BANF1 reported as likely benign for autosomal recessive disease

Included ClinVar conditions (1196):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 4
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HGVS dbSNP gnomAD frequency
NM_001143985.1(BANF1):c.-254G>T rs78790365 0.02064
NM_003860.4(BANF1):c.*100C>T rs145574018 0.00424
NM_001143985.1(BANF1):c.-297G>A rs141605220 0.00271
NM_003860.4(BANF1):c.*273C>G rs142270527 0.00037

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