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rs863224522

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224522(A;A)
Make rs863224522(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position76347454
GeneBBS10
is asnp
is mentioned by
dbSNPrs863224522
ebirs863224522
HLIrs863224522
Exacrs863224522
Varsomers863224522
Maprs863224522
PheGenIrs863224522
hapmaprs863224522
1000 genomesrs863224522
hgdprs863224522
ensemblrs863224522
gopubmedrs863224522
geneviewrs863224522
scholarrs863224522
googlers863224522
pharmgkbrs863224522
gwascentralrs863224522
openSNPrs863224522
23andMers863224522
23andMe allrs863224522
SNP Nexus

SNPshotrs863224522
SNPdbers863224522
MSV3drs863224522
GWAS Ctlgrs863224522
Max Magnitude0
ClinVar
Risk rs863224522(A;A)
Alt rs863224522(A;A)
Reference rs863224522(C;C)
Significance Pathogenic
Disease Bardet-Biedl syndrome
Variation info
Gene BBS10
CLNDBN Bardet-Biedl syndrome
Reversed 1
HGVS NC_000012.11:g.76741234G>T
CLNSRC
CLNACC RCV000196568.2,