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rs869025216

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869025216(A;G)
Make rs869025216(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position184170317
GeneDVL3
is asnp
is mentioned by
dbSNPrs869025216
ebirs869025216
HLIrs869025216
Exacrs869025216
Varsomers869025216
Maprs869025216
PheGenIrs869025216
hapmaprs869025216
1000 genomesrs869025216
hgdprs869025216
ensemblrs869025216
gopubmedrs869025216
geneviewrs869025216
scholarrs869025216
googlers869025216
pharmgkbrs869025216
gwascentralrs869025216
openSNPrs869025216
23andMers869025216
23andMe allrs869025216
SNP Nexus

SNPshotrs869025216
SNPdbers869025216
MSV3drs869025216
GWAS Ctlgrs869025216
Max Magnitude0
ClinVar
Risk rs869025216(G;G)
Alt rs869025216(G;G)
Reference rs869025216(A;A)
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.183888105A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000208665.1, RCV000210487.1,