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rs121918276

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121918276(A;C)
Make rs121918276(C;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position124868837
GeneROBO3
is asnp
is mentioned by
dbSNPrs121918276
ebirs121918276
HLIrs121918276
Exacrs121918276
Varsomers121918276
Maprs121918276
PheGenIrs121918276
hapmaprs121918276
1000 genomesrs121918276
hgdprs121918276
ensemblrs121918276
gopubmedrs121918276
geneviewrs121918276
scholarrs121918276
googlers121918276
pharmgkbrs121918276
gwascentralrs121918276
openSNPrs121918276
23andMers121918276
23andMe allrs121918276
SNP Nexus

SNPshotrs121918276
SNPdbers121918276
MSV3drs121918276
GWAS Ctlgrs121918276
Max Magnitude0
OMIM608630
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121918276(C;C)
Alt rs121918276(C;C)
Reference rs121918276(A;A)
Significance Pathogenic
Disease Gaze palsy
Variation info
Gene ROBO3
CLNDBN Gaze palsy, familial horizontal, with progressive scoliosis
Reversed 0
HGVS NC_000011.9:g.124738733A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000002264.4,