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rs529829552

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs529829552(C;T)
Make rs529829552(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position91724524
GeneROR2
is asnp
is mentioned by
dbSNPrs529829552
ebirs529829552
HLIrs529829552
Exacrs529829552
Varsomers529829552
Maprs529829552
PheGenIrs529829552
hapmaprs529829552
1000 genomesrs529829552
hgdprs529829552
ensemblrs529829552
gopubmedrs529829552
geneviewrs529829552
scholarrs529829552
googlers529829552
pharmgkbrs529829552
gwascentralrs529829552
openSNPrs529829552
23andMers529829552
23andMe allrs529829552
SNP Nexus

SNPshotrs529829552
SNPdbers529829552
MSV3drs529829552
GWAS Ctlgrs529829552
Max Magnitude0
ClinVar
Risk rs529829552(T;T)
Alt rs529829552(T;T)
Reference rs529829552(C;C)
Significance Probable-Pathogenic
Disease Brachydactyly not provided
Variation info
Gene ROR2
CLNDBN Brachydactyly, type B1Robinow syndrome, autosomal recessive not provided
Reversed 0
HGVS NC_000009.11:g.94486806C>T
CLNSRC
CLNACC RCV000147384.1, RCV000171424.1,