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rs772731615

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs772731615(C;T)
Make rs772731615(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position96860628
GeneVRK1
is asnp
is mentioned by
dbSNPrs772731615
ebirs772731615
HLIrs772731615
Exacrs772731615
Varsomers772731615
Maprs772731615
PheGenIrs772731615
hapmaprs772731615
1000 genomesrs772731615
hgdprs772731615
ensemblrs772731615
gopubmedrs772731615
geneviewrs772731615
scholarrs772731615
googlers772731615
pharmgkbrs772731615
gwascentralrs772731615
openSNPrs772731615
23andMers772731615
23andMe allrs772731615
SNP Nexus

SNPshotrs772731615
SNPdbers772731615
MSV3drs772731615
GWAS Ctlgrs772731615
Max Magnitude0
ClinVar
Risk rs772731615(T;T)
Alt rs772731615(T;T)
Reference rs772731615(C;C)
Significance Probable-Pathogenic
Disease Pontocerebellar hypoplasia type 1
Variation info
Gene VRK1
CLNDBN Pontocerebellar hypoplasia type 1
Reversed 0
HGVS NC_000014.8:g.97326965C>T
CLNSRC Baylor College of Medicine
CLNACC RCV000191144.1,