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rs1025884753

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position73473620
GeneMTO1
is asnp
is mentioned by
dbSNPrs1025884753
dbSNP (classic)rs1025884753
ClinGenrs1025884753
ebirs1025884753
HLIrs1025884753
Exacrs1025884753
Gnomadrs1025884753
Varsomers1025884753
LitVarrs1025884753
Maprs1025884753
PheGenIrs1025884753
Biobankrs1025884753
1000 genomesrs1025884753
hgdprs1025884753
ensemblrs1025884753
geneviewrs1025884753
scholarrs1025884753
googlers1025884753
pharmgkbrs1025884753
gwascentralrs1025884753
openSNPrs1025884753
23andMers1025884753
23andMe allrs1025884753
SNPshotrs1025884753
SNPdbers1025884753
MSV3drs1025884753
GWAS Ctlgrs1025884753
Max Magnitude0
ClinVar
Risk rs1025884753(T;T)
Alt rs1025884753(T;T)
Reference Rs1025884753(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.74183343C>T
CLNSRC
CLNACC RCV000489964.1,