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

rs121909082

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909082(A;A)
Make rs121909082(A;C)
ReferenceGRCh38 38.1/141
Chromosome9
Position91724229
GeneROR2
is asnp
is mentioned by
dbSNPrs121909082
ebirs121909082
HLIrs121909082
Exacrs121909082
Varsomers121909082
Maprs121909082
PheGenIrs121909082
hapmaprs121909082
1000 genomesrs121909082
hgdprs121909082
ensemblrs121909082
gopubmedrs121909082
geneviewrs121909082
scholarrs121909082
googlers121909082
pharmgkbrs121909082
gwascentralrs121909082
openSNPrs121909082
23andMers121909082
23andMe allrs121909082
SNP Nexus

SNPshotrs121909082
SNPdbers121909082
MSV3drs121909082
GWAS Ctlgrs121909082
Max Magnitude0
OMIM602337
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121909082(A,T;A,T)
Alt rs121909082(A,T;A,T)
Reference rs121909082(C;C)
Significance Pathogenic
Disease Brachydactyly type B1
Variation info
Gene ROR2
CLNDBN Brachydactyly type B1
Reversed 1
HGVS NC_000009.11:g.94486511G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007727.3,