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

rs869025215

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869025215(-;-)
Make rs869025215(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position184170092
GeneDVL3
is asnp
is mentioned by
dbSNPrs869025215
ebirs869025215
HLIrs869025215
Exacrs869025215
Varsomers869025215
Maprs869025215
PheGenIrs869025215
hapmaprs869025215
1000 genomesrs869025215
hgdprs869025215
ensemblrs869025215
gopubmedrs869025215
geneviewrs869025215
scholarrs869025215
googlers869025215
pharmgkbrs869025215
gwascentralrs869025215
openSNPrs869025215
23andMers869025215
23andMe allrs869025215
SNP Nexus

SNPshotrs869025215
SNPdbers869025215
MSV3drs869025215
GWAS Ctlgrs869025215
Max Magnitude0
ClinVar
Risk rs869025215(;)
Alt rs869025215(;)
Reference rs869025215(G;G)
Significance Pathogenic
Disease Robinow syndrome Robinow syndrome
Variation info
Gene DVL3
CLNDBN Robinow syndrome Robinow syndrome, autosomal dominant 3
Reversed 0
HGVS NC_000003.11:g.183887880delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000208632.1, RCV000210480.1,