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rs771364038

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs771364038(G;T)
Make rs771364038(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position96855353
GeneVRK1
is asnp
is mentioned by
dbSNPrs771364038
ebirs771364038
HLIrs771364038
Exacrs771364038
Varsomers771364038
Maprs771364038
PheGenIrs771364038
hapmaprs771364038
1000 genomesrs771364038
hgdprs771364038
ensemblrs771364038
gopubmedrs771364038
geneviewrs771364038
scholarrs771364038
googlers771364038
pharmgkbrs771364038
gwascentralrs771364038
openSNPrs771364038
23andMers771364038
23andMe allrs771364038
SNP Nexus

SNPshotrs771364038
SNPdbers771364038
MSV3drs771364038
GWAS Ctlgrs771364038
Max Magnitude0
ClinVar
Risk rs771364038(A,T;A,T)
Alt rs771364038(A,T;A,T)
Reference rs771364038(G;G)
Significance Pathogenic
Disease Pontocerebellar hypoplasia type 1
Variation info
Gene VRK1
CLNDBN Pontocerebellar hypoplasia type 1
Reversed 0
HGVS NC_000014.8:g.97321690G>A
CLNSRC
CLNACC RCV000203265.1,