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rs1060499776

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060499776(A;A)
Make rs1060499776(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position73497766
GeneMTO1
is asnp
is mentioned by
dbSNPrs1060499776
dbSNP (old)rs1060499776
ClinGenrs1060499776
ebirs1060499776
HLIrs1060499776
Exacrs1060499776
Gnomadrs1060499776
Varsomers1060499776
LitVarrs1060499776
Maprs1060499776
PheGenIrs1060499776
Biobankrs1060499776
1000 genomesrs1060499776
hgdprs1060499776
ensemblrs1060499776
gopubmedrs1060499776
geneviewrs1060499776
scholarrs1060499776
googlers1060499776
pharmgkbrs1060499776
gwascentralrs1060499776
openSNPrs1060499776
23andMers1060499776
23andMe allrs1060499776
SNPshotrs1060499776
SNPdbers1060499776
MSV3drs1060499776
GWAS Ctlgrs1060499776
Max Magnitude0
ClinVar
Risk rs1060499776(A;A)
Alt rs1060499776(A;A)
Reference Rs1060499776(T;T)
Significance Probable-Pathogenic
Disease Abnormality of brain morphology
Variation info
Gene MTO1
CLNDBN Abnormality of brain morphology
Reversed 0
HGVS NC_000006.11:g.74207489T>A
CLNSRC
CLNACC RCV000454152.1,