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rs1064794653

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome7
Position157005841
GeneMNX1, MNX1-AS2
is asnp
is mentioned by
dbSNPrs1064794653
dbSNP (old)rs1064794653
ClinGenrs1064794653
ebirs1064794653
HLIrs1064794653
Exacrs1064794653
Gnomadrs1064794653
Varsomers1064794653
LitVarrs1064794653
Maprs1064794653
PheGenIrs1064794653
Biobankrs1064794653
1000 genomesrs1064794653
hgdprs1064794653
ensemblrs1064794653
gopubmedrs1064794653
geneviewrs1064794653
scholarrs1064794653
googlers1064794653
pharmgkbrs1064794653
gwascentralrs1064794653
openSNPrs1064794653
23andMers1064794653
23andMe allrs1064794653
SNPshotrs1064794653
SNPdbers1064794653
MSV3drs1064794653
GWAS Ctlgrs1064794653
Max Magnitude0
ClinVar
Risk rs1064794653(C;C)
Alt rs1064794653(C;C)
Reference Rs1064794653(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MNX1-AS2 MNX1
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.156798535T>G
CLNSRC
CLNACC RCV000479220.1,