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

rs1064794855

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
ChromosomeX
Position153866831
GeneL1CAM
is asnp
is mentioned by
dbSNPrs1064794855
dbSNP (old)rs1064794855
ClinGenrs1064794855
ebirs1064794855
HLIrs1064794855
Exacrs1064794855
Gnomadrs1064794855
Varsomers1064794855
Maprs1064794855
PheGenIrs1064794855
Biobankrs1064794855
1000 genomesrs1064794855
hgdprs1064794855
ensemblrs1064794855
gopubmedrs1064794855
geneviewrs1064794855
scholarrs1064794855
googlers1064794855
pharmgkbrs1064794855
gwascentralrs1064794855
openSNPrs1064794855
23andMers1064794855
23andMe allrs1064794855
SNPshotrs1064794855
SNPdbers1064794855
MSV3drs1064794855
GWAS Ctlgrs1064794855
Max Magnitude0
ClinVar
Risk rs1064794855(C;C)
Alt rs1064794855(C;C)
Reference Rs1064794855(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene L1CAM
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153132286T>G
CLNSRC
CLNACC RCV000483657.1,