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rs1057516861

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057516861(-;GT)
Make rs1057516861(GT;GT)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position76347769
GeneBBS10
is asnp
is mentioned by
dbSNPrs1057516861
dbSNP (old)rs1057516861
ClinGenrs1057516861
ebirs1057516861
HLIrs1057516861
Exacrs1057516861
Gnomadrs1057516861
Varsomers1057516861
LitVarrs1057516861
Maprs1057516861
PheGenIrs1057516861
Biobankrs1057516861
1000 genomesrs1057516861
hgdprs1057516861
ensemblrs1057516861
gopubmedrs1057516861
geneviewrs1057516861
scholarrs1057516861
googlers1057516861
pharmgkbrs1057516861
gwascentralrs1057516861
openSNPrs1057516861
23andMers1057516861
23andMe allrs1057516861
SNPshotrs1057516861
SNPdbers1057516861
MSV3drs1057516861
GWAS Ctlgrs1057516861
Max Magnitude0
ClinVar
Risk rs1057516861(GT;GT)
Alt rs1057516861(GT;GT)
Reference Rs1057516861(-;-)
Significance Probable-Pathogenic
Disease Bardet-Biedl syndrome 10
Variation info
Gene BBS10
CLNDBN Bardet-Biedl syndrome 10
Reversed 1
HGVS NC_000012.11:g.76741550_76741551dupAC
CLNSRC
CLNACC RCV000409141.1,