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rs137852857

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852857(A;A)
Make rs137852857(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position33177570
GeneBBS9
is asnp
is mentioned by
dbSNPrs137852857
ebirs137852857
HLIrs137852857
Exacrs137852857
Varsomers137852857
Maprs137852857
PheGenIrs137852857
hapmaprs137852857
1000 genomesrs137852857
hgdprs137852857
ensemblrs137852857
gopubmedrs137852857
geneviewrs137852857
scholarrs137852857
googlers137852857
pharmgkbrs137852857
gwascentralrs137852857
openSNPrs137852857
23andMers137852857
23andMe allrs137852857
SNP Nexus

SNPshotrs137852857
SNPdbers137852857
MSV3drs137852857
GWAS Ctlgrs137852857
Max Magnitude0
OMIM607968
Desc
Variant0004
Relatedalso
ClinVar
Risk rs137852857(A;A)
Alt rs137852857(A;A)
Reference rs137852857(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.33217182G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000002778.4,