Have questions? Visit https://www.reddit.com/r/SNPedia

rs761101213

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs761101213(-;-)
Make rs761101213(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position76347298
GeneBBS10
is asnp
is mentioned by
dbSNPrs761101213
dbSNP (old)rs761101213
ClinGenrs761101213
ebirs761101213
HLIrs761101213
Exacrs761101213
Gnomadrs761101213
Varsomers761101213
Maprs761101213
PheGenIrs761101213
Biobankrs761101213
1000 genomesrs761101213
hgdprs761101213
ensemblrs761101213
gopubmedrs761101213
geneviewrs761101213
scholarrs761101213
googlers761101213
pharmgkbrs761101213
gwascentralrs761101213
openSNPrs761101213
23andMers761101213
23andMe allrs761101213
SNP Nexus

SNPshotrs761101213
SNPdbers761101213
MSV3drs761101213
GWAS Ctlgrs761101213
Max Magnitude0
ClinVar
Risk rs761101213(-;-)
Alt rs761101213(-;-)
Reference Rs761101213(A;A)
Significance Pathogenic
Disease Bardet-Biedl syndrome Bardet-Biedl syndrome 10
Variation info
Gene BBS10
CLNDBN Bardet-Biedl syndrome Bardet-Biedl syndrome 10
Reversed 0
HGVS NC_000012.11:g.76741078delA
CLNSRC
CLNACC RCV000197461.2, RCV000401310.1,