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rs267607016

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607016(C;T)
Make rs267607016(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position91726603
GeneROR2
is asnp
is mentioned by
dbSNPrs267607016
ebirs267607016
HLIrs267607016
Exacrs267607016
Varsomers267607016
Maprs267607016
PheGenIrs267607016
hapmaprs267607016
1000 genomesrs267607016
hgdprs267607016
ensemblrs267607016
gopubmedrs267607016
geneviewrs267607016
scholarrs267607016
googlers267607016
pharmgkbrs267607016
gwascentralrs267607016
openSNPrs267607016
23andMers267607016
23andMe allrs267607016
SNP Nexus

SNPshotrs267607016
SNPdbers267607016
MSV3drs267607016
GWAS Ctlgrs267607016
Max Magnitude0
ClinVar
Risk rs267607016(T;T)
Alt rs267607016(T;T)
Reference rs267607016(C;C)
Significance Pathogenic
Disease Robinow syndrome
Variation info
Gene ROR2
CLNDBN Robinow syndrome, autosomal recessive, with brachy-syn-polydactyly
Reversed 1
HGVS NC_000009.11:g.94488885G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007742.5,