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rs121909087

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909087(C;T)
Make rs121909087(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position91757380
GeneROR2
is asnp
is mentioned by
dbSNPrs121909087
ebirs121909087
HLIrs121909087
Exacrs121909087
Varsomers121909087
Maprs121909087
PheGenIrs121909087
hapmaprs121909087
1000 genomesrs121909087
hgdprs121909087
ensemblrs121909087
gopubmedrs121909087
geneviewrs121909087
scholarrs121909087
googlers121909087
pharmgkbrs121909087
gwascentralrs121909087
openSNPrs121909087
23andMers121909087
23andMe allrs121909087
SNP Nexus

SNPshotrs121909087
SNPdbers121909087
MSV3drs121909087
GWAS Ctlgrs121909087
Max Magnitude0
OMIM602337
Desc
Variant0011
Relatedalso
ClinVar
Risk rs121909087(T;T)
Alt rs121909087(T;T)
Reference Rs121909087(C;C)
Significance Pathogenic
Disease Robinow syndrome not provided
Variation info
Gene ROR2
CLNDBN Robinow syndrome, autosomal recessive not provided
Reversed 1
HGVS NC_000009.11:g.94519662G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007738.4, RCV000238984.1,