Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057516998

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GA;GA) 0 common in clinvar
Make rs1057516998(-;-)
Make rs1057516998(-;GA)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position76346972
GeneBBS10
is asnp
is mentioned by
dbSNPrs1057516998
dbSNP (old)rs1057516998
ClinGenrs1057516998
ebirs1057516998
HLIrs1057516998
Exacrs1057516998
Gnomadrs1057516998
Varsomers1057516998
Maprs1057516998
PheGenIrs1057516998
Biobankrs1057516998
1000 genomesrs1057516998
hgdprs1057516998
ensemblrs1057516998
gopubmedrs1057516998
geneviewrs1057516998
scholarrs1057516998
googlers1057516998
pharmgkbrs1057516998
gwascentralrs1057516998
openSNPrs1057516998
23andMers1057516998
23andMe allrs1057516998
SNPshotrs1057516998
SNPdbers1057516998
MSV3drs1057516998
GWAS Ctlgrs1057516998
Max Magnitude0
ClinVar
Risk rs1057516998(-;-)
Alt rs1057516998(-;-)
Reference Rs1057516998(GA;GA)
Significance Probable-Pathogenic
Disease Bardet-Biedl syndrome 10
Variation info
Gene BBS10
CLNDBN Bardet-Biedl syndrome 10
Reversed 1
HGVS NC_000012.11:g.76740752_76740753delTC
CLNSRC
CLNACC RCV000410766.1,