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rs869025211

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869025211(-;-)
Make rs869025211(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position76346438
GeneBBS10
is asnp
is mentioned by
dbSNPrs869025211
ebirs869025211
HLIrs869025211
Exacrs869025211
Varsomers869025211
Maprs869025211
PheGenIrs869025211
hapmaprs869025211
1000 genomesrs869025211
hgdprs869025211
ensemblrs869025211
gopubmedrs869025211
geneviewrs869025211
scholarrs869025211
googlers869025211
pharmgkbrs869025211
gwascentralrs869025211
openSNPrs869025211
23andMers869025211
23andMe allrs869025211
SNP Nexus

SNPshotrs869025211
SNPdbers869025211
MSV3drs869025211
GWAS Ctlgrs869025211
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs869025211(C;C)
Significance Pathogenic
Disease Bardet-Biedl syndrome 10
Variation info
Gene BBS10
CLNDBN Bardet-Biedl syndrome 10
Reversed 1
HGVS NC_000012.11:g.76740218delG
CLNSRC
CLNACC RCV000207760.1,