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rs797044948

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797044948(A;G)
Make rs797044948(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position46671766
GeneVPS35
is asnp
is mentioned by
dbSNPrs797044948
ebirs797044948
HLIrs797044948
Exacrs797044948
Varsomers797044948
Maprs797044948
PheGenIrs797044948
hapmaprs797044948
1000 genomesrs797044948
hgdprs797044948
ensemblrs797044948
gopubmedrs797044948
geneviewrs797044948
scholarrs797044948
googlers797044948
pharmgkbrs797044948
gwascentralrs797044948
openSNPrs797044948
23andMers797044948
23andMe allrs797044948
SNP Nexus

SNPshotrs797044948
SNPdbers797044948
MSV3drs797044948
GWAS Ctlgrs797044948
Max Magnitude0
ClinVar
Risk rs797044948(G;G)
Alt rs797044948(G;G)
Reference rs797044948(A;A)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene VPS35
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000016.9:g.46705678T>C
CLNSRC
CLNACC RCV000190799.1,