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rs797044838

From SNPedia

Orientationminus
Make rs797044838(-;-)
Make rs797044838(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position1338087
GeneDVL1
is asnp
is mentioned by
dbSNPrs797044838
ebirs797044838
HLIrs797044838
Exacrs797044838
Varsomers797044838
Maprs797044838
PheGenIrs797044838
hapmaprs797044838
1000 genomesrs797044838
hgdprs797044838
ensemblrs797044838
gopubmedrs797044838
geneviewrs797044838
scholarrs797044838
googlers797044838
pharmgkbrs797044838
gwascentralrs797044838
openSNPrs797044838
23andMers797044838
23andMe allrs797044838
SNP Nexus

SNPshotrs797044838
SNPdbers797044838
MSV3drs797044838
GWAS Ctlgrs797044838
Max Magnitude
ClinVar
Risk rs797044838(;)
Alt rs797044838(;)
Reference rs797044838(G;G)
Significance Pathogenic
Disease Robinow syndrome
Variation info
Gene DVL1
CLNDBN Robinow syndrome, autosomal dominant 2
Reversed 1
HGVS NC_000001.10:g.1273467delC
CLNSRC
CLNACC RCV000195217.1,