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rs869025218

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869025218(-;-)
Make rs869025218(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position184170320
GeneDVL3
is asnp
is mentioned by
dbSNPrs869025218
ebirs869025218
HLIrs869025218
Exacrs869025218
Varsomers869025218
Maprs869025218
PheGenIrs869025218
hapmaprs869025218
1000 genomesrs869025218
hgdprs869025218
ensemblrs869025218
gopubmedrs869025218
geneviewrs869025218
scholarrs869025218
googlers869025218
pharmgkbrs869025218
gwascentralrs869025218
openSNPrs869025218
23andMers869025218
23andMe allrs869025218
SNP Nexus

SNPshotrs869025218
SNPdbers869025218
MSV3drs869025218
GWAS Ctlgrs869025218
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs869025218(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.183888108delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000208637.1, RCV000210486.1,