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rs770556842

From SNPedia

Orientationplus
Geno Mag Summary
(AGTT;AGTT) 0 common in clinvar
Make rs770556842(-;-)
Make rs770556842(-;AGTT)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position76346383
GeneBBS10
is asnp
is mentioned by
dbSNPrs770556842
ebirs770556842
HLIrs770556842
Exacrs770556842
Varsomers770556842
Maprs770556842
PheGenIrs770556842
hapmaprs770556842
1000 genomesrs770556842
hgdprs770556842
ensemblrs770556842
gopubmedrs770556842
geneviewrs770556842
scholarrs770556842
googlers770556842
pharmgkbrs770556842
gwascentralrs770556842
openSNPrs770556842
23andMers770556842
23andMe allrs770556842
SNP Nexus

SNPshotrs770556842
SNPdbers770556842
MSV3drs770556842
GWAS Ctlgrs770556842
Max Magnitude0
ClinVar
Risk rs770556842(;)
Alt rs770556842(;)
Reference rs770556842(AGTT;AGTT)
Significance Probable-Pathogenic
Disease Bardet-Biedl syndrome 10
Variation info
Gene BBS10
CLNDBN Bardet-Biedl syndrome 10
Reversed 0
HGVS NC_000012.11:g.76740163_76740166delAGTT
CLNSRC
CLNACC RCV000169372.1,