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rs773864735

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs773864735(-;-)
Make rs773864735(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position76346452
GeneBBS10
is asnp
is mentioned by
dbSNPrs773864735
dbSNP (classic)rs773864735
ClinGenrs773864735
ebirs773864735
HLIrs773864735
Exacrs773864735
Gnomadrs773864735
Varsomers773864735
LitVarrs773864735
Maprs773864735
PheGenIrs773864735
Biobankrs773864735
1000 genomesrs773864735
hgdprs773864735
ensemblrs773864735
geneviewrs773864735
scholarrs773864735
googlers773864735
pharmgkbrs773864735
gwascentralrs773864735
openSNPrs773864735
23andMers773864735
SNPshotrs773864735
SNPdbers773864735
MSV3drs773864735
GWAS Ctlgrs773864735
Max Magnitude0
ClinVar
Risk rs773864735(-;-)
Alt rs773864735(-;-)
Reference Rs773864735(C;C)
Significance Probable-Pathogenic
Disease Bardet-Biedl syndrome 10
Variation info
Gene BBS10
CLNDBN Bardet-Biedl syndrome 10
Reversed 0
HGVS NC_000012.11:g.76740232delC
CLNSRC
CLNACC RCV000412206.1,