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rs587777810

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587777810(-;-)
Make rs587777810(-;C)
Make rs587777810(C;C)
ReferenceGRCh38 38.1/142
Chromosome7
Position33388074
GeneBBS9
is asnp
is mentioned by
dbSNPrs587777810
ebirs587777810
HLIrs587777810
Exacrs587777810
Varsomers587777810
Maprs587777810
PheGenIrs587777810
hapmaprs587777810
1000 genomesrs587777810
hgdprs587777810
ensemblrs587777810
gopubmedrs587777810
geneviewrs587777810
scholarrs587777810
googlers587777810
pharmgkbrs587777810
gwascentralrs587777810
openSNPrs587777810
23andMers587777810
23andMe allrs587777810
SNP Nexus

SNPshotrs587777810
SNPdbers587777810
MSV3drs587777810
GWAS Ctlgrs587777810
Max Magnitude0
ClinVar
Risk rs587777810(C;C)
Alt rs587777810(C;C)
Reference rs587777810(;)
Significance Pathogenic
Disease Bardet-Biedl syndrome 9
Variation info
Gene BBS9
CLNDBN Bardet-Biedl syndrome 9
Reversed 0
HGVS NC_000007.13:g.33427686dupC
CLNSRC OMIM Allelic Variant
CLNACC RCV000002777.4,