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rs768933093

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs768933093(A;A)
Make rs768933093(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position76348214
GeneBBS10
is asnp
is mentioned by
dbSNPrs768933093
ebirs768933093
HLIrs768933093
Exacrs768933093
Varsomers768933093
Maprs768933093
PheGenIrs768933093
hapmaprs768933093
1000 genomesrs768933093
hgdprs768933093
ensemblrs768933093
gopubmedrs768933093
geneviewrs768933093
scholarrs768933093
googlers768933093
pharmgkbrs768933093
gwascentralrs768933093
openSNPrs768933093
23andMers768933093
23andMe allrs768933093
SNP Nexus

SNPshotrs768933093
SNPdbers768933093
MSV3drs768933093
GWAS Ctlgrs768933093
Max Magnitude0
ClinVar
Risk rs768933093(A;A)
Alt rs768933093(A;A)
Reference rs768933093(G;G)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene BBS10
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000012.11:g.76741994G>A
CLNSRC
CLNACC RCV000210662.1,