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rs1060499779

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499779(A;A)
Make rs1060499779(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position99013791
GeneLOC105375666, VPS13B
is asnp
is mentioned by
dbSNPrs1060499779
dbSNP (old)rs1060499779
ClinGenrs1060499779
ebirs1060499779
HLIrs1060499779
Exacrs1060499779
Gnomadrs1060499779
Varsomers1060499779
LitVarrs1060499779
Maprs1060499779
PheGenIrs1060499779
Biobankrs1060499779
1000 genomesrs1060499779
hgdprs1060499779
ensemblrs1060499779
gopubmedrs1060499779
geneviewrs1060499779
scholarrs1060499779
googlers1060499779
pharmgkbrs1060499779
gwascentralrs1060499779
openSNPrs1060499779
23andMers1060499779
23andMe allrs1060499779
SNPshotrs1060499779
SNPdbers1060499779
MSV3drs1060499779
GWAS Ctlgrs1060499779
Max Magnitude0
ClinVar
Risk rs1060499779(A;A)
Alt rs1060499779(A;A)
Reference Rs1060499779(G;G)
Significance Probable-Pathogenic
Disease Abnormality of brain morphology
Variation info
Gene VPS13B
CLNDBN Abnormality of brain morphology
Reversed 0
HGVS NC_000008.10:g.100026019G>A
CLNSRC
CLNACC RCV000454311.1,