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rs869025205

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869025205(C;T)
Make rs869025205(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position66523784
GeneBBS1, ZDHHC24
is asnp
is mentioned by
dbSNPrs869025205
ebirs869025205
HLIrs869025205
Exacrs869025205
Varsomers869025205
Maprs869025205
PheGenIrs869025205
hapmaprs869025205
1000 genomesrs869025205
hgdprs869025205
ensemblrs869025205
gopubmedrs869025205
geneviewrs869025205
scholarrs869025205
googlers869025205
pharmgkbrs869025205
gwascentralrs869025205
openSNPrs869025205
23andMers869025205
23andMe allrs869025205
SNP Nexus

SNPshotrs869025205
SNPdbers869025205
MSV3drs869025205
GWAS Ctlgrs869025205
Max Magnitude0
ClinVar
Risk rs869025205(T;T)
Alt rs869025205(T;T)
Reference rs869025205(C;C)
Significance Pathogenic
Disease Bardet-Biedl syndrome
Variation info
Gene BBS1 ZDHHC24
CLNDBN Bardet-Biedl syndrome
Reversed 0
HGVS NC_000011.9:g.66291255C>T
CLNSRC
CLNACC RCV000207577.1,