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rs199474722

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199474722(A;A)
Make rs199474722(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position76346783
GeneBBS10
is asnp
is mentioned by
dbSNPrs199474722
ebirs199474722
HLIrs199474722
Exacrs199474722
Varsomers199474722
Maprs199474722
PheGenIrs199474722
hapmaprs199474722
1000 genomesrs199474722
hgdprs199474722
ensemblrs199474722
gopubmedrs199474722
geneviewrs199474722
scholarrs199474722
googlers199474722
pharmgkbrs199474722
gwascentralrs199474722
openSNPrs199474722
23andMers199474722
23andMe allrs199474722
SNP Nexus

SNPshotrs199474722
SNPdbers199474722
MSV3drs199474722
GWAS Ctlgrs199474722
Max Magnitude0
ClinVar
Risk rs199474722(A;A)
Alt rs199474722(A;A)
Reference rs199474722(G;G)
Significance Pathogenic
Disease Bardet-Biedl syndrome 10
Variation info
Gene BBS10
CLNDBN Bardet-Biedl syndrome 10
Reversed 1
HGVS NC_000012.11:g.76740563C>T
CLNSRC ClinVar
CLNACC RCV000058867.1,