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rs1057516266

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(ATTT;ATTT) 0 common in clinvar
Make rs1057516266(-;-)
Make rs1057516266(-;ATTT)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position76347414
GeneBBS10
is asnp
is mentioned by
dbSNPrs1057516266
dbSNP (old)rs1057516266
ClinGenrs1057516266
ebirs1057516266
HLIrs1057516266
Exacrs1057516266
Gnomadrs1057516266
Varsomers1057516266
Maprs1057516266
PheGenIrs1057516266
Biobankrs1057516266
1000 genomesrs1057516266
hgdprs1057516266
ensemblrs1057516266
gopubmedrs1057516266
geneviewrs1057516266
scholarrs1057516266
googlers1057516266
pharmgkbrs1057516266
gwascentralrs1057516266
openSNPrs1057516266
23andMers1057516266
23andMe allrs1057516266
SNPshotrs1057516266
SNPdbers1057516266
MSV3drs1057516266
GWAS Ctlgrs1057516266
Max Magnitude0
ClinVar
Risk rs1057516266(-;-)
Alt rs1057516266(-;-)
Reference Rs1057516266(ATTT;ATTT)
Significance Probable-Pathogenic
Disease Bardet-Biedl syndrome 10
Variation info
Gene BBS10
CLNDBN Bardet-Biedl syndrome 10
Reversed 1
HGVS NC_000012.11:g.76741194_76741197delAAAT
CLNSRC
CLNACC RCV000411390.1,