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rs878855095

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878855095(A;A)
Make rs878855095(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position66514662
GeneBBS1
is asnp
is mentioned by
dbSNPrs878855095
ClinGenrs878855095
ebirs878855095
HLIrs878855095
Exacrs878855095
Varsomers878855095
Maprs878855095
PheGenIrs878855095
hapmaprs878855095
1000 genomesrs878855095
hgdprs878855095
ensemblrs878855095
gopubmedrs878855095
geneviewrs878855095
scholarrs878855095
googlers878855095
pharmgkbrs878855095
gwascentralrs878855095
openSNPrs878855095
23andMers878855095
23andMe allrs878855095
SNP Nexus

SNPshotrs878855095
SNPdbers878855095
MSV3drs878855095
GWAS Ctlgrs878855095
Max Magnitude0
ClinVar
Risk rs878855095(A;A)
Alt rs878855095(A;A)
Reference Rs878855095(G;G)
Significance Pathogenic
Disease Bardet-Biedl syndrome
Variation info
Gene BBS1
CLNDBN Bardet-Biedl syndrome
Reversed 0
HGVS NC_000011.9:g.66282133G>A
CLNSRC
CLNACC RCV000230074.1,