Have questions? Visit https://www.reddit.com/r/SNPedia

rs797044836

From SNPedia

Orientationminus
Make rs797044836(-;-)
Make rs797044836(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position1338108
GeneDVL1
is asnp
is mentioned by
dbSNPrs797044836
ebirs797044836
HLIrs797044836
Exacrs797044836
Varsomers797044836
Maprs797044836
PheGenIrs797044836
hapmaprs797044836
1000 genomesrs797044836
hgdprs797044836
ensemblrs797044836
gopubmedrs797044836
geneviewrs797044836
scholarrs797044836
googlers797044836
pharmgkbrs797044836
gwascentralrs797044836
openSNPrs797044836
23andMers797044836
23andMe allrs797044836
SNP Nexus

SNPshotrs797044836
SNPdbers797044836
MSV3drs797044836
GWAS Ctlgrs797044836
Max Magnitude
ClinVar
Risk rs797044836(;)
Alt rs797044836(;)
Reference rs797044836(C;C)
Significance Pathogenic
Disease Robinow syndrome
Variation info
Gene DVL1
CLNDBN Robinow syndrome, autosomal dominant 2
Reversed 1
HGVS NC_000001.10:g.1273488delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000192930.3,