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rs1057516628

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057516628(-;-)
Make rs1057516628(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position76346026
GeneBBS10
is asnp
is mentioned by
dbSNPrs1057516628
dbSNP (old)rs1057516628
ClinGenrs1057516628
ebirs1057516628
HLIrs1057516628
Exacrs1057516628
Gnomadrs1057516628
Varsomers1057516628
Maprs1057516628
PheGenIrs1057516628
Biobankrs1057516628
1000 genomesrs1057516628
hgdprs1057516628
ensemblrs1057516628
gopubmedrs1057516628
geneviewrs1057516628
scholarrs1057516628
googlers1057516628
pharmgkbrs1057516628
gwascentralrs1057516628
openSNPrs1057516628
23andMers1057516628
23andMe allrs1057516628
SNPshotrs1057516628
SNPdbers1057516628
MSV3drs1057516628
GWAS Ctlgrs1057516628
Max Magnitude0
ClinVar
Risk rs1057516628(-;-)
Alt rs1057516628(-;-)
Reference Rs1057516628(C;C)
Significance Probable-Pathogenic
Disease Bardet-Biedl syndrome 10
Variation info
Gene BBS10
CLNDBN Bardet-Biedl syndrome 10
Reversed 1
HGVS NC_000012.11:g.76739806delG
CLNSRC
CLNACC RCV000410373.1,