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rs121909083

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909083(C;T)
Make rs121909083(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position91724990
GeneROR2
is asnp
is mentioned by
dbSNPrs121909083
ebirs121909083
HLIrs121909083
Exacrs121909083
Varsomers121909083
Maprs121909083
PheGenIrs121909083
hapmaprs121909083
1000 genomesrs121909083
hgdprs121909083
ensemblrs121909083
gopubmedrs121909083
geneviewrs121909083
scholarrs121909083
googlers121909083
pharmgkbrs121909083
gwascentralrs121909083
openSNPrs121909083
23andMers121909083
23andMe allrs121909083
SNP Nexus

SNPshotrs121909083
SNPdbers121909083
MSV3drs121909083
GWAS Ctlgrs121909083
Max Magnitude0
OMIM602337
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121909083(T;T)
Alt rs121909083(T;T)
Reference rs121909083(C;C)
Significance Pathogenic
Disease Robinow syndrome
Variation info
Gene ROR2
CLNDBN Robinow syndrome, autosomal recessive
Reversed 1
HGVS NC_000009.11:g.94487272G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007730.3,