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rs1060499734

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060499734(C;T)
Make rs1060499734(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position31780935
GeneVARS
is asnp
is mentioned by
dbSNPrs1060499734
dbSNP (old)rs1060499734
ClinGenrs1060499734
ebirs1060499734
HLIrs1060499734
Exacrs1060499734
Gnomadrs1060499734
Varsomers1060499734
Maprs1060499734
PheGenIrs1060499734
Biobankrs1060499734
1000 genomesrs1060499734
hgdprs1060499734
ensemblrs1060499734
gopubmedrs1060499734
geneviewrs1060499734
scholarrs1060499734
googlers1060499734
pharmgkbrs1060499734
gwascentralrs1060499734
openSNPrs1060499734
23andMers1060499734
23andMe allrs1060499734
SNPshotrs1060499734
SNPdbers1060499734
MSV3drs1060499734
GWAS Ctlgrs1060499734
Max Magnitude0
ClinVar
Risk rs1060499734(T;T)
Alt rs1060499734(T;T)
Reference Rs1060499734(C;C)
Significance Probable-Pathogenic
Disease Abnormality of brain morphology
Variation info
Gene VARS
CLNDBN Abnormality of brain morphology
Reversed 1
HGVS NC_000006.11:g.31748712G>A
CLNSRC
CLNACC RCV000454203.1,