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rs587777811

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777811(C;C)
Make rs587777811(C;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position33177592
GeneBBS9
is asnp
is mentioned by
dbSNPrs587777811
ebirs587777811
HLIrs587777811
Exacrs587777811
Varsomers587777811
Maprs587777811
PheGenIrs587777811
hapmaprs587777811
1000 genomesrs587777811
hgdprs587777811
ensemblrs587777811
gopubmedrs587777811
geneviewrs587777811
scholarrs587777811
googlers587777811
pharmgkbrs587777811
gwascentralrs587777811
openSNPrs587777811
23andMers587777811
23andMe allrs587777811
SNP Nexus

SNPshotrs587777811
SNPdbers587777811
MSV3drs587777811
GWAS Ctlgrs587777811
Max Magnitude0
ClinVar
Risk rs587777811(C;C)
Alt rs587777811(C;C)
Reference rs587777811(G;G)
Significance Pathogenic
Disease Bardet-Biedl syndrome 9
Variation info
Gene BBS9
CLNDBN Bardet-Biedl syndrome 9
Reversed 0
HGVS NC_000007.13:g.33217204G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000002780.4,