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rs869025219

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869025219(-;-)
Make rs869025219(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position184170353
GeneDVL3
is asnp
is mentioned by
dbSNPrs869025219
ebirs869025219
HLIrs869025219
Exacrs869025219
Varsomers869025219
Maprs869025219
PheGenIrs869025219
hapmaprs869025219
1000 genomesrs869025219
hgdprs869025219
ensemblrs869025219
gopubmedrs869025219
geneviewrs869025219
scholarrs869025219
googlers869025219
pharmgkbrs869025219
gwascentralrs869025219
openSNPrs869025219
23andMers869025219
23andMe allrs869025219
SNP Nexus

SNPshotrs869025219
SNPdbers869025219
MSV3drs869025219
GWAS Ctlgrs869025219
Max Magnitude0
ClinVar
Risk rs869025219(;)
Alt rs869025219(;)
Reference rs869025219(C;C)
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.183888141delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000208671.1, RCV000210482.1,