Have questions? Visit https://www.reddit.com/r/SNPedia

rs869025210

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs869025210(-;-)
Make rs869025210(-;A)
Make rs869025210(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position76346960
GeneBBS10
is asnp
is mentioned by
dbSNPrs869025210
ebirs869025210
HLIrs869025210
Exacrs869025210
Varsomers869025210
Maprs869025210
PheGenIrs869025210
hapmaprs869025210
1000 genomesrs869025210
hgdprs869025210
ensemblrs869025210
gopubmedrs869025210
geneviewrs869025210
scholarrs869025210
googlers869025210
pharmgkbrs869025210
gwascentralrs869025210
openSNPrs869025210
23andMers869025210
23andMe allrs869025210
SNP Nexus

SNPshotrs869025210
SNPdbers869025210
MSV3drs869025210
GWAS Ctlgrs869025210
Max Magnitude0
ClinVar
Risk rs869025210(A;A)
Alt rs869025210(A;A)
Reference rs869025210(;)
Significance Pathogenic
Disease Bardet-Biedl syndrome 10
Variation info
Gene BBS10
CLNDBN Bardet-Biedl syndrome 10
Reversed 1
HGVS NC_000012.11:g.76740741dupT
CLNSRC
CLNACC RCV000207540.1,