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rs137852858

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852858(C;T)
Make rs137852858(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position33336487
GeneBBS9
is asnp
is mentioned by
dbSNPrs137852858
ebirs137852858
HLIrs137852858
Exacrs137852858
Varsomers137852858
Maprs137852858
PheGenIrs137852858
hapmaprs137852858
1000 genomesrs137852858
hgdprs137852858
ensemblrs137852858
gopubmedrs137852858
geneviewrs137852858
scholarrs137852858
googlers137852858
pharmgkbrs137852858
gwascentralrs137852858
openSNPrs137852858
23andMers137852858
23andMe allrs137852858
SNP Nexus

SNPshotrs137852858
SNPdbers137852858
MSV3drs137852858
GWAS Ctlgrs137852858
Max Magnitude0
OMIM607968
Desc
Variant0005
Relatedalso
ClinVar
Risk rs137852858(T;T)
Alt rs137852858(T;T)
Reference rs137852858(C;C)
Significance Pathogenic
Disease Bardet-Biedl syndrome 9
Variation info
Gene BBS9
CLNDBN Bardet-Biedl syndrome 9
Reversed 0
HGVS NC_000007.13:g.33376099C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000002779.4,