Have questions? Visit https://www.reddit.com/r/SNPedia

rs121909085

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909085(A;A)
Make rs121909085(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position91724334
GeneROR2
is asnp
is mentioned by
dbSNPrs121909085
ebirs121909085
HLIrs121909085
Exacrs121909085
Varsomers121909085
Maprs121909085
PheGenIrs121909085
hapmaprs121909085
1000 genomesrs121909085
hgdprs121909085
ensemblrs121909085
gopubmedrs121909085
geneviewrs121909085
scholarrs121909085
googlers121909085
pharmgkbrs121909085
gwascentralrs121909085
openSNPrs121909085
23andMers121909085
23andMe allrs121909085
SNP Nexus

SNPshotrs121909085
SNPdbers121909085
MSV3drs121909085
GWAS Ctlgrs121909085
Max Magnitude0
OMIM602337
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121909085(A;A)
Alt rs121909085(A;A)
Reference rs121909085(G;G)
Significance Pathogenic
Disease Robinow syndrome
Variation info
Gene ROR2
CLNDBN Robinow syndrome, autosomal recessive
Reversed 1
HGVS NC_000009.11:g.94486616C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007732.3,