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rs121909084

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909084(C;T)
Make rs121909084(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position91737463
GeneROR2
is asnp
is mentioned by
dbSNPrs121909084
ebirs121909084
HLIrs121909084
Exacrs121909084
Varsomers121909084
Maprs121909084
PheGenIrs121909084
hapmaprs121909084
1000 genomesrs121909084
hgdprs121909084
ensemblrs121909084
gopubmedrs121909084
geneviewrs121909084
scholarrs121909084
googlers121909084
pharmgkbrs121909084
gwascentralrs121909084
openSNPrs121909084
23andMers121909084
23andMe allrs121909084
SNP Nexus

SNPshotrs121909084
SNPdbers121909084
MSV3drs121909084
GWAS Ctlgrs121909084
Max Magnitude0
OMIM602337
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121909084(T;T)
Alt rs121909084(T;T)
Reference rs121909084(C;C)
Significance Pathogenic
Disease Robinow syndrome
Variation info
Gene ROR2
CLNDBN Robinow syndrome, autosomal recessive
Reversed 1
HGVS NC_000009.11:g.94499745G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007731.4,