ClinVar Miner

List of variants reported as pathogenic for Bardet-Biedl syndrome by Advanced Center For Translational And Genetic Medicine, Ann & Robert H. Lurie Children's Hospital Of Chicago

Included ClinVar conditions (45):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 10
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HGVS dbSNP gnomAD frequency
NM_024649.5(BBS1):c.1169T>G (p.Met390Arg) rs113624356 0.00212
NM_152384.3(BBS5):c.619-1G>C rs753234582 0.00004
NM_033028.5(BBS4):c.332+8T>C rs1456405256 0.00001
NM_152618.3(BBS12):c.1063C>T (p.Arg355Ter) rs121918327 0.00001
GRCh37/hg19 11q13.2(chr11:66274870-66292647)x1
GRCh37/hg19 15q24.1(chr15:73000552-73006857)x1
GRCh37/hg19 2q13(chr2:110875689-110967529)
NM_152618.3(BBS12):c.1392_1395del (p.Cys464fs) rs2150737232
NM_152618.3(BBS12):c.1685del (p.Asn562fs)
NM_176824.3(BBS7):c.712_715del (p.Arg238fs) rs760165634

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