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rs1064793163

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
ChromosomeX
Position153868699
GeneL1CAM
is asnp
is mentioned by
dbSNPrs1064793163
dbSNP (old)rs1064793163
ClinGenrs1064793163
ebirs1064793163
HLIrs1064793163
Exacrs1064793163
Gnomadrs1064793163
Varsomers1064793163
Maprs1064793163
PheGenIrs1064793163
Biobankrs1064793163
1000 genomesrs1064793163
hgdprs1064793163
ensemblrs1064793163
gopubmedrs1064793163
geneviewrs1064793163
scholarrs1064793163
googlers1064793163
pharmgkbrs1064793163
gwascentralrs1064793163
openSNPrs1064793163
23andMers1064793163
23andMe allrs1064793163
SNPshotrs1064793163
SNPdbers1064793163
MSV3drs1064793163
GWAS Ctlgrs1064793163
Max Magnitude0
ClinVar
Risk rs1064793163(T;T)
Alt rs1064793163(T;T)
Reference Rs1064793163(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene L1CAM
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153134154G>A
CLNSRC
CLNACC RCV000487331.1,