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rs863223291

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(ACAAGCT;ACAAGCT) 0 common in clinvar
Make rs863223291(-;-)
Make rs863223291(-;ACAAGCT)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position91724551
GeneROR2
is asnp
is mentioned by
dbSNPrs863223291
dbSNP (old)rs863223291
ClinGenrs863223291
ebirs863223291
HLIrs863223291
Exacrs863223291
Gnomadrs863223291
Varsomers863223291
Maprs863223291
PheGenIrs863223291
Biobankrs863223291
1000 genomesrs863223291
hgdprs863223291
ensemblrs863223291
gopubmedrs863223291
geneviewrs863223291
scholarrs863223291
googlers863223291
pharmgkbrs863223291
gwascentralrs863223291
openSNPrs863223291
23andMers863223291
23andMe allrs863223291
SNP Nexus

SNPshotrs863223291
SNPdbers863223291
MSV3drs863223291
GWAS Ctlgrs863223291
Max Magnitude0
ClinVar
Risk rs863223291(-;-)
Alt rs863223291(-;-)
Reference Rs863223291(ACAAGCT;ACAAGCT)
Significance Pathogenic
Disease Robinow syndrome
Variation info
Gene ROR2
CLNDBN Robinow syndrome, autosomal recessive
Reversed 1
HGVS NC_000009.11:g.94486833_94486839delAGCTTGT
CLNSRC OMIM Allelic Variant
CLNACC RCV000007737.3,