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rs869312959

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312959(A;A)
Make rs869312959(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position96860736
GeneVRK1
is asnp
is mentioned by
dbSNPrs869312959
ebirs869312959
HLIrs869312959
Exacrs869312959
Varsomers869312959
Maprs869312959
PheGenIrs869312959
hapmaprs869312959
1000 genomesrs869312959
hgdprs869312959
ensemblrs869312959
gopubmedrs869312959
geneviewrs869312959
scholarrs869312959
googlers869312959
pharmgkbrs869312959
gwascentralrs869312959
openSNPrs869312959
23andMers869312959
23andMe allrs869312959
SNP Nexus

SNPshotrs869312959
SNPdbers869312959
MSV3drs869312959
GWAS Ctlgrs869312959
Max Magnitude0
ClinVar
Risk rs869312959(A;A)
Alt rs869312959(A;A)
Reference rs869312959(G;G)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene VRK1
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000014.8:g.97327073G>A
CLNSRC
CLNACC RCV000210540.1,