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rs121918274

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918274(A;A)
Make rs121918274(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position124870650
GeneROBO3
is asnp
is mentioned by
dbSNPrs121918274
ebirs121918274
HLIrs121918274
Exacrs121918274
Varsomers121918274
Maprs121918274
PheGenIrs121918274
hapmaprs121918274
1000 genomesrs121918274
hgdprs121918274
ensemblrs121918274
gopubmedrs121918274
geneviewrs121918274
scholarrs121918274
googlers121918274
pharmgkbrs121918274
gwascentralrs121918274
openSNPrs121918274
23andMers121918274
23andMe allrs121918274
SNP Nexus

SNPshotrs121918274
SNPdbers121918274
MSV3drs121918274
GWAS Ctlgrs121918274
Max Magnitude0
OMIM608630
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121918274(A,C;A,C)
Alt rs121918274(A,C;A,C)
Reference rs121918274(G;G)
Significance Pathogenic
Disease Gaze palsy
Variation info
Gene ROBO3
CLNDBN Gaze palsy, familial horizontal, with progressive scoliosis
Reversed 0
HGVS NC_000011.9:g.124740546G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000002261.4,