ClinVar Miner

List of variants reported as likely benign for Bardet-Biedl syndrome 1 by Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 8
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HGVS dbSNP gnomAD frequency
NM_031885.5(BBS2):c.1413A>C (p.Val471=) rs35294865 0.01415
NM_015910.7(WDPCP):c.2063A>G (p.Asn688Ser) rs61734468 0.00905
NM_152618.3(BBS12):c.714T>G (p.Asn238Lys) rs17006082 0.00860
NM_176824.3(BBS7):c.1512-7A>T rs115987385 0.00545
NM_031885.5(BBS2):c.1422G>A (p.Ser474=) rs117033008 0.00250
NM_024649.5(BBS1):c.1719A>G (p.Gln573=) rs150553044 0.00194
NM_024685.4(BBS10):c.765G>A (p.Met255Ile) rs139658279 0.00072
NM_015910.7(WDPCP):c.1448G>A (p.Arg483Gln) rs544657165 0.00001

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