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rs869025209

From SNPedia

Orientationminus
Geno Mag Summary
(AAAAATGCCA;AAAAATGCCA) 0 common in clinvar
Make rs869025209(-;-)
Make rs869025209(-;AAAAATGCCA)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position76346120
GeneBBS10
is asnp
is mentioned by
dbSNPrs869025209
ebirs869025209
HLIrs869025209
Exacrs869025209
Varsomers869025209
Maprs869025209
PheGenIrs869025209
hapmaprs869025209
1000 genomesrs869025209
hgdprs869025209
ensemblrs869025209
gopubmedrs869025209
geneviewrs869025209
scholarrs869025209
googlers869025209
pharmgkbrs869025209
gwascentralrs869025209
openSNPrs869025209
23andMers869025209
23andMe allrs869025209
SNP Nexus

SNPshotrs869025209
SNPdbers869025209
MSV3drs869025209
GWAS Ctlgrs869025209
Max Magnitude0
ClinVar
Risk rs869025209(;)
Alt rs869025209(;)
Reference rs869025209(AAAAATGCCA;AAAAATGCCA)
Significance Pathogenic
Disease Bardet-Biedl syndrome 10
Variation info
Gene BBS10
CLNDBN Bardet-Biedl syndrome 10
Reversed 1
HGVS NC_000012.11:g.76739900_76739909delTGGCATTTTT
CLNSRC
CLNACC RCV000207911.1,