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rs121909086

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909086(C;T)
Make rs121909086(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position91737400
GeneROR2
is asnp
is mentioned by
dbSNPrs121909086
ebirs121909086
HLIrs121909086
Exacrs121909086
Varsomers121909086
Maprs121909086
PheGenIrs121909086
hapmaprs121909086
1000 genomesrs121909086
hgdprs121909086
ensemblrs121909086
gopubmedrs121909086
geneviewrs121909086
scholarrs121909086
googlers121909086
pharmgkbrs121909086
gwascentralrs121909086
openSNPrs121909086
23andMers121909086
23andMe allrs121909086
SNP Nexus

SNPshotrs121909086
SNPdbers121909086
MSV3drs121909086
GWAS Ctlgrs121909086
Max Magnitude0
OMIM602337
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121909086(A,T;A,T)
Alt rs121909086(A,T;A,T)
Reference rs121909086(C;C)
Significance Pathogenic
Disease Robinow syndrome
Variation info
Gene ROR2
CLNDBN Robinow syndrome, autosomal recessive
Reversed 1
HGVS NC_000009.11:g.94499682G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007733.4,