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rs869025217

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869025217(A;A)
Make rs869025217(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position184170318
GeneDVL3
is asnp
is mentioned by
dbSNPrs869025217
ebirs869025217
HLIrs869025217
Exacrs869025217
Varsomers869025217
Maprs869025217
PheGenIrs869025217
hapmaprs869025217
1000 genomesrs869025217
hgdprs869025217
ensemblrs869025217
gopubmedrs869025217
geneviewrs869025217
scholarrs869025217
googlers869025217
pharmgkbrs869025217
gwascentralrs869025217
openSNPrs869025217
23andMers869025217
23andMe allrs869025217
SNP Nexus

SNPshotrs869025217
SNPdbers869025217
MSV3drs869025217
GWAS Ctlgrs869025217
Max Magnitude0
ClinVar
Risk rs869025217(A;A)
Alt rs869025217(A;A)
Reference rs869025217(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.183888106G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000208714.1, RCV000210483.1,