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rs863224534

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224534(G;T)
Make rs863224534(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position33349161
GeneBBS9
is asnp
is mentioned by
dbSNPrs863224534
ebirs863224534
HLIrs863224534
Exacrs863224534
Varsomers863224534
Maprs863224534
PheGenIrs863224534
hapmaprs863224534
1000 genomesrs863224534
hgdprs863224534
ensemblrs863224534
gopubmedrs863224534
geneviewrs863224534
scholarrs863224534
googlers863224534
pharmgkbrs863224534
gwascentralrs863224534
openSNPrs863224534
23andMers863224534
23andMe allrs863224534
SNP Nexus

SNPshotrs863224534
SNPdbers863224534
MSV3drs863224534
GWAS Ctlgrs863224534
Max Magnitude0
ClinVar
Risk rs863224534(T;T)
Alt rs863224534(T;T)
Reference rs863224534(G;G)
Significance Pathogenic
Disease Bardet-Biedl syndrome
Variation info
Gene BBS9
CLNDBN Bardet-Biedl syndrome
Reversed 0
HGVS NC_000007.13:g.33388773G>T
CLNSRC
CLNACC RCV000195839.2,