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rs137852856

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852856(C;T)
Make rs137852856(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position33383668
GeneBBS9
is asnp
is mentioned by
dbSNPrs137852856
ebirs137852856
HLIrs137852856
Exacrs137852856
Varsomers137852856
Maprs137852856
PheGenIrs137852856
hapmaprs137852856
1000 genomesrs137852856
hgdprs137852856
ensemblrs137852856
gopubmedrs137852856
geneviewrs137852856
scholarrs137852856
googlers137852856
pharmgkbrs137852856
gwascentralrs137852856
openSNPrs137852856
23andMers137852856
23andMe allrs137852856
SNP Nexus

SNPshotrs137852856
SNPdbers137852856
MSV3drs137852856
GWAS Ctlgrs137852856
Max Magnitude0
OMIM607968
Desc
Variant0002
Relatedalso
ClinVar
Risk rs137852856(T;T)
Alt rs137852856(T;T)
Reference rs137852856(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.33423280C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000002776.4,