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rs137962929

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137962929(A;A)
Make rs137962929(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position33152852
GeneBBS9
is asnp
is mentioned by
dbSNPrs137962929
dbSNP (old)rs137962929
ClinGenrs137962929
ebirs137962929
HLIrs137962929
Exacrs137962929
Gnomadrs137962929
Varsomers137962929
Maprs137962929
PheGenIrs137962929
Biobankrs137962929
1000 genomesrs137962929
hgdprs137962929
ensemblrs137962929
gopubmedrs137962929
geneviewrs137962929
scholarrs137962929
googlers137962929
pharmgkbrs137962929
gwascentralrs137962929
openSNPrs137962929
23andMers137962929
23andMe allrs137962929
SNPshotrs137962929
SNPdbers137962929
MSV3drs137962929
GWAS Ctlgrs137962929
Max Magnitude0
ClinVar
Risk rs137962929(A;A)
Alt rs137962929(A;A)
Reference Rs137962929(G;G)
Significance Pathogenic
Disease Bardet-Biedl syndrome
Variation info
Gene BBS9
CLNDBN Bardet-Biedl syndrome
Reversed 0
HGVS NC_000007.13:g.33192464G>A
CLNSRC
CLNACC RCV000477579.1,