Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1064796665

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome7
Position157006520
GeneMNX1, MNX1-AS2
is asnp
is mentioned by
dbSNPrs1064796665
dbSNP (old)rs1064796665
ClinGenrs1064796665
ebirs1064796665
HLIrs1064796665
Exacrs1064796665
Gnomadrs1064796665
Varsomers1064796665
Maprs1064796665
PheGenIrs1064796665
Biobankrs1064796665
1000 genomesrs1064796665
hgdprs1064796665
ensemblrs1064796665
gopubmedrs1064796665
geneviewrs1064796665
scholarrs1064796665
googlers1064796665
pharmgkbrs1064796665
gwascentralrs1064796665
openSNPrs1064796665
23andMers1064796665
23andMe allrs1064796665
SNPshotrs1064796665
SNPdbers1064796665
MSV3drs1064796665
GWAS Ctlgrs1064796665
Max Magnitude0
ClinVar
Risk rs1064796665(-;-)
Alt rs1064796665(-;-)
Reference Rs1064796665(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MNX1-AS2 MNX1
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.156799214delG
CLNSRC
CLNACC RCV000487416.1,