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rs1064793162

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
ChromosomeX
Position153869928
GeneL1CAM
is asnp
is mentioned by
dbSNPrs1064793162
dbSNP (old)rs1064793162
ClinGenrs1064793162
ebirs1064793162
HLIrs1064793162
Exacrs1064793162
Gnomadrs1064793162
Varsomers1064793162
Maprs1064793162
PheGenIrs1064793162
Biobankrs1064793162
1000 genomesrs1064793162
hgdprs1064793162
ensemblrs1064793162
gopubmedrs1064793162
geneviewrs1064793162
scholarrs1064793162
googlers1064793162
pharmgkbrs1064793162
gwascentralrs1064793162
openSNPrs1064793162
23andMers1064793162
23andMe allrs1064793162
SNPshotrs1064793162
SNPdbers1064793162
MSV3drs1064793162
GWAS Ctlgrs1064793162
Max Magnitude0
ClinVar
Risk rs1064793162(G;G)
Alt rs1064793162(G;G)
Reference Rs1064793162(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene L1CAM
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153135383G>C
CLNSRC
CLNACC RCV000484845.1,