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rs797044835

From SNPedia

Orientationminus
Make rs797044835(-;-)
Make rs797044835(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position1338097
GeneDVL1
is asnp
is mentioned by
dbSNPrs797044835
ebirs797044835
HLIrs797044835
Exacrs797044835
Varsomers797044835
Maprs797044835
PheGenIrs797044835
hapmaprs797044835
1000 genomesrs797044835
hgdprs797044835
ensemblrs797044835
gopubmedrs797044835
geneviewrs797044835
scholarrs797044835
googlers797044835
pharmgkbrs797044835
gwascentralrs797044835
openSNPrs797044835
23andMers797044835
23andMe allrs797044835
SNP Nexus

SNPshotrs797044835
SNPdbers797044835
MSV3drs797044835
GWAS Ctlgrs797044835
Max Magnitude
ClinVar
Risk rs797044835(;)
Alt rs797044835(;)
Reference rs797044835(T;T)
Significance Pathogenic
Disease Robinow syndrome
Variation info
Gene DVL1
CLNDBN Robinow syndrome, autosomal dominant 2
Reversed 1
HGVS NC_000001.10:g.1273477delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000195250.3,