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rs762511626

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs762511626(A;A)
Make rs762511626(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position33349108
GeneBBS9
is asnp
is mentioned by
dbSNPrs762511626
ebirs762511626
HLIrs762511626
Exacrs762511626
Varsomers762511626
Maprs762511626
PheGenIrs762511626
hapmaprs762511626
1000 genomesrs762511626
hgdprs762511626
ensemblrs762511626
gopubmedrs762511626
geneviewrs762511626
scholarrs762511626
googlers762511626
pharmgkbrs762511626
gwascentralrs762511626
openSNPrs762511626
23andMers762511626
23andMe allrs762511626
SNP Nexus

SNPshotrs762511626
SNPdbers762511626
MSV3drs762511626
GWAS Ctlgrs762511626
Max Magnitude0
ClinVar
Risk rs762511626(A;A)
Alt rs762511626(A;A)
Reference rs762511626(T;T)
Significance Pathogenic
Disease Bardet-Biedl syndrome
Variation info
Gene BBS9
CLNDBN Bardet-Biedl syndrome
Reversed 0
HGVS NC_000007.13:g.33388720T>A
CLNSRC
CLNACC RCV000199446.1,