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rs137852836

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852836(C;C)
Make rs137852836(C;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position76348258
GeneBBS10
is asnp
is mentioned by
dbSNPrs137852836
ebirs137852836
HLIrs137852836
Exacrs137852836
Varsomers137852836
Maprs137852836
PheGenIrs137852836
hapmaprs137852836
1000 genomesrs137852836
hgdprs137852836
ensemblrs137852836
gopubmedrs137852836
geneviewrs137852836
scholarrs137852836
googlers137852836
pharmgkbrs137852836
gwascentralrs137852836
openSNPrs137852836
23andMers137852836
23andMe allrs137852836
SNP Nexus

SNPshotrs137852836
SNPdbers137852836
MSV3drs137852836
GWAS Ctlgrs137852836
Max Magnitude0
OMIM610148
Desc
Variant0002
Relatedalso
ClinVar
Risk rs137852836(C;C)
Alt rs137852836(C;C)
Reference rs137852836(G;G)
Significance Pathogenic
Disease Bardet-Biedl syndrome 10
Variation info
Gene BBS10
CLNDBN Bardet-Biedl syndrome 10
Reversed 1
HGVS NC_000012.11:g.76742038C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000001392.4,