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rs797044837

From SNPedia

Orientationminus
Make rs797044837(-;-)
Make rs797044837(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position1338001
GeneDVL1
is asnp
is mentioned by
dbSNPrs797044837
ebirs797044837
HLIrs797044837
Exacrs797044837
Varsomers797044837
Maprs797044837
PheGenIrs797044837
hapmaprs797044837
1000 genomesrs797044837
hgdprs797044837
ensemblrs797044837
gopubmedrs797044837
geneviewrs797044837
scholarrs797044837
googlers797044837
pharmgkbrs797044837
gwascentralrs797044837
openSNPrs797044837
23andMers797044837
23andMe allrs797044837
SNP Nexus

SNPshotrs797044837
SNPdbers797044837
MSV3drs797044837
GWAS Ctlgrs797044837
Max Magnitude
ClinVar
Risk rs797044837(;)
Alt rs797044837(;)
Reference rs797044837(A;A)
Significance Pathogenic
Disease Robinow syndrome
Variation info
Gene DVL1
CLNDBN Robinow syndrome, autosomal dominant 2
Reversed 1
HGVS NC_000001.10:g.1273381delT
CLNSRC
CLNACC RCV000193819.1,