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rs1057517206

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TA;TA) 0 common in clinvar
Make rs1057517206(-;-)
Make rs1057517206(-;TA)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position76346794
GeneBBS10
is asnp
is mentioned by
dbSNPrs1057517206
dbSNP (old)rs1057517206
ClinGenrs1057517206
ebirs1057517206
HLIrs1057517206
Exacrs1057517206
Gnomadrs1057517206
Varsomers1057517206
LitVarrs1057517206
Maprs1057517206
PheGenIrs1057517206
Biobankrs1057517206
1000 genomesrs1057517206
hgdprs1057517206
ensemblrs1057517206
gopubmedrs1057517206
geneviewrs1057517206
scholarrs1057517206
googlers1057517206
pharmgkbrs1057517206
gwascentralrs1057517206
openSNPrs1057517206
23andMers1057517206
23andMe allrs1057517206
SNPshotrs1057517206
SNPdbers1057517206
MSV3drs1057517206
GWAS Ctlgrs1057517206
Max Magnitude0
ClinVar
Risk rs1057517206(-;-)
Alt rs1057517206(-;-)
Reference Rs1057517206(TA;TA)
Significance Probable-Pathogenic
Disease Bardet-Biedl syndrome 10
Variation info
Gene BBS10
CLNDBN Bardet-Biedl syndrome 10
Reversed 1
HGVS NC_000012.11:g.76740574_76740575delTA
CLNSRC
CLNACC RCV000409409.1,