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rs141970072

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs141970072(A;A)
Make rs141970072(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position73482170
GeneMTO1
is asnp
is mentioned by
dbSNPrs141970072
dbSNP (classic)rs141970072
ClinGenrs141970072
ebirs141970072
HLIrs141970072
Exacrs141970072
Gnomadrs141970072
Varsomers141970072
LitVarrs141970072
Maprs141970072
PheGenIrs141970072
Biobankrs141970072
1000 genomesrs141970072
hgdprs141970072
ensemblrs141970072
geneviewrs141970072
scholarrs141970072
googlers141970072
pharmgkbrs141970072
gwascentralrs141970072
openSNPrs141970072
23andMers141970072
23andMe allrs141970072
SNPshotrs141970072
SNPdbers141970072
MSV3drs141970072
GWAS Ctlgrs141970072
Max Magnitude0
ClinVar
Risk rs141970072(A;A) rs141970072(T;T)
Alt rs141970072(A;A) rs141970072(T;T)
Reference Rs141970072(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MTO1
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.74191893G>T
CLNSRC
CLNACC RCV000481072.1,